NDC 68382-898 – Tadalafil
Tadalafil 10 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-898
Product details
- Brand name
- Tadalafil
- Generic name
- Tadalafil
- Labeler
- Zydus Pharmaceuticals USA Inc.
- 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 10 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68382-898-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-898-01) | Mar 27, 2019 |
| 68382-898-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-898-05) | Mar 27, 2019 |
| 68382-898-06 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-898-06) | Mar 27, 2019 |
| 68382-898-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-898-10) | Mar 27, 2019 |
| 68382-898-16 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-898-16) | Mar 27, 2019 |
| 68382-898-99 | 2 BLISTER PACK in 1 CARTON (68382-898-99) / 15 TABLET, FILM COATED in 1 BLISTER PACK | Mar 27, 2019 |
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