United States · FDA National Drug Code directory
Tadalafil
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70771-1477_89266030-a1a1-4825-b9f0-9400886b6282
- Product NDC
- 70771-1477
- Form
- TABLET, FILM COATED
- Composition / generic term
- Tadalafil
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190327
- Source listing expiry
- 20261231
Source-listed ingredients
- TADALAFIL — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1477-0) · 70771-1477-0
- 100 TABLET, FILM COATED in 1 BOTTLE (70771-1477-1) · 70771-1477-1
- 30 TABLET, FILM COATED in 1 BOTTLE (70771-1477-3) · 70771-1477-3
- 2 BLISTER PACK in 1 CARTON (70771-1477-4) / 15 TABLET, FILM COATED in 1 BLISTER PACK · 70771-1477-4
- 500 TABLET, FILM COATED in 1 BOTTLE (70771-1477-5) · 70771-1477-5
- 90 TABLET, FILM COATED in 1 BOTTLE (70771-1477-9) · 70771-1477-9
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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