NDC 70771-1478 – Tadalafil
Tadalafil 20 mg/1 · Tablet, Film Coated · Oral
Product NDC70771-1478
Product details
- Brand name
- Tadalafil
- Generic name
- Tadalafil
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206693
- Marketed since
- March 27, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Tadalafil 20 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1478-0 | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1478-0) | Mar 27, 2019 |
| 70771-1478-1 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1478-1) | Mar 27, 2019 |
| 70771-1478-3 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1478-3) | Mar 27, 2019 |
| 70771-1478-4 | 2 BLISTER PACK in 1 CARTON (70771-1478-4) / 15 TABLET, FILM COATED in 1 BLISTER PACK | Mar 27, 2019 |
| 70771-1478-5 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1478-5) | Mar 27, 2019 |
| 70771-1478-9 | 90 TABLET, FILM COATED in 1 BOTTLE (70771-1478-9) | Mar 27, 2019 |
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