Sealed 25 kg drum of tadalafil API (CAS 171596-29-5) - Pharmint pack
Illustrative pack rendering - request formal pack-shot for tender
Active Pharmaceutical Ingredient

Tadalafil API - Bulk Powder

WHO-GMPEU-GMPUS-FDA registered facility

High-purity tadalafil API for licensed formulators. Ships from India-based GMP-audited facilities with Certificate of Analysis and DMF letter of access. Pharmacopeial grades (USP / EP / BP) available on request.

Price on request
Quoted per SKU, quantity, and destination
Grade
BP
Pack size
1 kg
SKU
TAD-API-BP-1KG
Request quote for this variant

B2B bulk enquiries only. No online purchase available.

Product specifications

Specifications
CAS number
171596-29-5
Grade / Strength
USP · EP · BP
Pack sizes
1 kg · 5 kg · 25 kg
Origin
GMP-audited manufacturer
For buyers in
United States (B2B)
Compliance
WHO-GMP · EU-GMP · US-FDA registered facility
Documentation on request
  • Certificate of Analysis (per lot)
  • Impurity profile
  • Manufacturer's DMF letter of access (under NDA)
  • Retest / stability data
  • MSDS

All variants (9)

Full SKU reference. Use the selector above to build a quote for a specific variant.

SKUDescriptionAvailability
TAD-API-USP-1KGUSP grade · 1 kgAvailable
TAD-API-USP-5KGUSP grade · 5 kgAvailable
TAD-API-USP-25KGUSP grade · 25 kgAvailable
TAD-API-EP-1KGEP grade · 1 kgAvailable
TAD-API-EP-5KGEP grade · 5 kgAvailable
TAD-API-EP-25KGEP grade · 25 kgAvailable
TAD-API-BP-1KGBP grade · 1 kgAvailable
TAD-API-BP-5KGBP grade · 5 kgAvailable
TAD-API-BP-25KGBP grade · 25 kgAvailable

Request quote

Confirm the SKU, tell us the quantity and destination, and we'll come back with pricing, lead time, and payment terms within one business day.

B2B only. Orders are accepted from licensed pharmaceutical wholesalers, importers, formulators, and manufacturers. Every enquiry passes a compliance review before dispatch.

  • Buyer licence verified before dispatch
  • Wire, LC, or net-30 for verified accounts
  • Full documentation (CoA, GMP, batch records) with every shipment
  • One business-day reply for standard SKUs
Regulatory & buyer information

Optional now - PHARMINT PTE. LTD. will verify these before dispatch. Providing them upfront speeds up the compliance review.

We reply with pricing, lead time, and payment terms within one business day. No payment collected on this page.

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

Apex Biopharma
Meridian Labs
Redline Pharma
Veritas Health
Kinesis Therapeutics
Northshore Rx
Apex Biopharma
Meridian Labs
Redline Pharma
Veritas Health
Kinesis Therapeutics
Northshore Rx
Apex Biopharma
Meridian Labs
Redline Pharma
Veritas Health
Kinesis Therapeutics
Northshore Rx
Apex Biopharma
Meridian Labs
Redline Pharma
Veritas Health
Kinesis Therapeutics
Northshore Rx