NDC 71335-1620 – Tadalafil
Tadalafil 10 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1620
Product details
- Brand name
- Tadalafil
- Generic name
- Tadalafil
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209167
- Marketed since
- April 3, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Tadalafil 10 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1620-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1620-1) | Jun 24, 2020 |
| 71335-1620-2 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1620-2) | Aug 20, 2020 |
| 71335-1620-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1620-3) | Jan 13, 2021 |
| 71335-1620-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1620-4) | Jun 3, 2020 |
| 71335-1620-5 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1620-5) | Oct 31, 2024 |
| 71335-1620-6 | 6 TABLET, FILM COATED in 1 BOTTLE (71335-1620-6) | Oct 31, 2024 |
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