Tadalafil API - Bulk Powder
Active pharmaceutical ingredient for licensed formulators. Ships with CoA and DMF letter of access.
- CAS
- 171596-29-5
- Grades
- USP · EP · BP
- Pack sizes
- 1 kg · 5 kg · 25 kg
WHO-GMPEU-GMPUS-FDA facility
For US importers & wholesalers
Tadalafil, sourced directly from India-based manufacturers.
Bulk API powder, finished-dose tablets, and combo tablets - with full documentation (CoA, CoPP, DMF letter of access) and US-import support.
- ✓ USP · EP · BP grades
- ✓ WHO-GMP manufacturers
- ✓ CoA per lot
- ✓ Reply < 1 business day
Product overview
- Substance
- Tadalafil
- CAS
- 171596-29-5
- Grades
- USP · EP · BP
- Formats
- API · Tablets · Combo
- Origin
- India (GMP-audited)
- Buyers
- United States (B2B)
- Docs
- CoA · CoPP · DMF
Products we source
Three formats to fit how you buy - API for your own formulation, finished tablets for resale, or combination tablets for regulated tender.
Tadalafil Tablets - Finished Dose
Generic film-coated tablets, blister-packed. Private-label and custom-strength runs available on MOQ.
- Strengths
- 2.5 / 5 / 10 / 20 mg
- Packs
- 4 / 10 / 30 tabs
- Docs
- CoA · CoPP · Stability
WHO-GMPEU-GMP optionsPrivate label
Tadalafil + Dapoxetine Combo
Fixed-dose combination tablets for regulated and semi-regulated markets. Full dossier available for tender.
- Strengths
- 20/30 mg · 20/60 mg
- Packs
- 4 / 10 tabs
- Docs
- CoA · Dossier
WHO-GMPTender-ready
Request quote
Tell us what you need. We reply within one business day with pricing, lead time, payment terms, and the documentation package - then ship on your confirmation.
B2B only. Orders are accepted from licensed pharmaceutical wholesalers, importers, formulators, and manufacturers. Every enquiry passes a compliance review before dispatch - see how we vet buyers.
Prefer email? Write to quotes@tadalafil-seller.com.
- ✓ Bulk orders for licensed importers, wholesalers & manufacturers
- ✓ Documentation shared under NDA where required
- ✓ Flexible payment terms - wire, LC, or net-30 for verified accounts
How buying from us works
Straight sourcing, honest paperwork, no consumer chatter.
- 1
Send us your requirements
Use the quote form: SKU, quantity, target destination, any documentation you need. Takes 60 seconds.
- 2
We source and price
We check availability with 2-3 GMP-audited manufacturers in India and come back with landed-cost pricing.
- 3
You review documentation
CoA, CoPP, DMF letter of access, stability data - shared under NDA where required.
- 4
Order, ship, land
We coordinate with your licensed customs broker for FDA prior-notice, shipping documents, and cold-chain if needed.
GMP audits
WHO · EU · US-FDA
Every source facility we work with is currently registered.
Documentation
Full paper trail
CoA per lot, CoPP, DMF LoA where applicable, stability data.
Reply time
1 business day
For quotes on standard SKUs. Custom runs may take longer.
Operating record
The numbers behind the sourcing desk
Two things buyers ask on every first call. Here's where we land, drawn from the last 12 months of dispatched enquiries.
Loading chart…
Every standard-SKU enquiry receives a first quote reply within one business day. Of those replies: 42% went out within 4 hours, 38% within 4 to 8 hours, 17% within 8 to 24 hours, and 3% at the one-business-day mark. Custom runs, dossier-tender enquiries, and RFQs requiring supplier callback are excluded and quoted on a case-by-case timeline.
Loading chart…
Every source facility on our active routing list holds a current WHO-GMP audit. 62% additionally hold an EU-GMP audit and 44% are additionally US-FDA-registered establishments. Facilities may hold more than one credential; the bars show coverage rates, not market share.
Reply-time measured from enquiry receipt to first outbound quote email on standard-SKU RFQs; custom-formulation and tender-dossier enquiries are excluded and quoted case by case. GMP-audit coverage counts each active facility once per credential held - a single facility can (and often does) hold multiple credentials, so the doughnut segments are coverage rates, not market shares.
What US buyers say
Trusted by licensed importers, wholesalers & formulators across the United States
Feedback from procurement and regulatory leads at B2B pharmaceutical buyers who have completed at least one dispatched order.
We've moved three tadalafil API tenders through them in the last year. CoAs match the third-party lab retest every time, and net-30 kicked in on our second PO. Our regulatory team stopped asking questions after the first DMF letter of access came through.
Daniel Weiss
Head of Procurement · Cascadia Formulations
Portland, OR
Straightforward B2B relationship. They asked for our wholesale distributor licence upfront, verified it against the state board, and only then shared pricing. Refreshing after dealing with brokers who ship first and worry about compliance later.
Priya Balachandran
Director of Sourcing · Meridian Pharma Wholesale
Edison, NJ
Quoted a 25 kg USP-grade lot on a Tuesday, had impurity profile and stability data in our inbox Wednesday morning, wire terms finalized Thursday. Lead time held. This is what the whole industry should look like.
Marcus Halloran
VP Supply Chain · Northshore Rx Manufacturing
Waukegan, IL
We were sceptical about India-origin API for our 505(b)(2) filing. They walked us through the WHO-GMP audit report, arranged a virtual facility tour with the manufacturer, and matched the reference-listed drug's impurity spec. Passed our internal QA gate first pass.
Aisha Rahman
Regulatory Affairs Lead · Apex Biopharma Sciences
Cambridge, MA
Tender documentation package was tight - CoPP, BMR excerpt, artwork proofs for our private-label run - all delivered within the window. Their ops team actually understands what a US repackager needs, we didn't have to explain 21 CFR Part 211 to anyone.
Robert Chen
Purchasing Manager · Veritas Health Distributors
Fremont, CA
Placed a modest first order to test the process. No pressure to upsize, no phantom minimum quantities that magically appeared later. Second order was 4x the first and pricing scaled cleanly. Referred two other formulators in our network.
Jennifer Osei
Chief Operating Officer · Redline Pharma Partners
Atlanta, GA
The compliance-review step slowed us down initially and we pushed back. In hindsight it's exactly why we now trust them - every shipment lands with the right paperwork, no customs holds, no surprise re-testing charges. Predictability is worth the extra 48 hours upfront.
Thomas Reilly
Director of Operations · Kinesis Therapeutics
Raleigh, NC
We've moved three tadalafil API tenders through them in the last year. CoAs match the third-party lab retest every time, and net-30 kicked in on our second PO. Our regulatory team stopped asking questions after the first DMF letter of access came through.
Daniel Weiss
Head of Procurement · Cascadia Formulations
Portland, OR
Straightforward B2B relationship. They asked for our wholesale distributor licence upfront, verified it against the state board, and only then shared pricing. Refreshing after dealing with brokers who ship first and worry about compliance later.
Priya Balachandran
Director of Sourcing · Meridian Pharma Wholesale
Edison, NJ
Quoted a 25 kg USP-grade lot on a Tuesday, had impurity profile and stability data in our inbox Wednesday morning, wire terms finalized Thursday. Lead time held. This is what the whole industry should look like.
Marcus Halloran
VP Supply Chain · Northshore Rx Manufacturing
Waukegan, IL
We were sceptical about India-origin API for our 505(b)(2) filing. They walked us through the WHO-GMP audit report, arranged a virtual facility tour with the manufacturer, and matched the reference-listed drug's impurity spec. Passed our internal QA gate first pass.
Aisha Rahman
Regulatory Affairs Lead · Apex Biopharma Sciences
Cambridge, MA
Tender documentation package was tight - CoPP, BMR excerpt, artwork proofs for our private-label run - all delivered within the window. Their ops team actually understands what a US repackager needs, we didn't have to explain 21 CFR Part 211 to anyone.
Robert Chen
Purchasing Manager · Veritas Health Distributors
Fremont, CA
Placed a modest first order to test the process. No pressure to upsize, no phantom minimum quantities that magically appeared later. Second order was 4x the first and pricing scaled cleanly. Referred two other formulators in our network.
Jennifer Osei
Chief Operating Officer · Redline Pharma Partners
Atlanta, GA
The compliance-review step slowed us down initially and we pushed back. In hindsight it's exactly why we now trust them - every shipment lands with the right paperwork, no customs holds, no surprise re-testing charges. Predictability is worth the extra 48 hours upfront.
Thomas Reilly
Director of Operations · Kinesis Therapeutics
Raleigh, NC
Selected B2B customers
Serving licensed pharmaceutical buyers across the US
