NDC 71205-268 – Tadalafil
Tadalafil 20 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-268
Product details
- Brand name
- Tadalafil
- Generic name
- Tadalafil
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209167
- Marketed since
- March 27, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Tadalafil 20 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71205-268-10 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-268-10) | Jul 1, 2019 |
| 71205-268-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-268-30) | May 1, 2019 |
| 71205-268-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-268-60) | May 1, 2019 |
| 71205-268-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-268-90) | May 1, 2019 |
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