NDC 71205-088 – Sildenafil
Sildenafil Citrate 100 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-088
Product details
- Brand name
- Sildenafil
- Generic name
- Sildenafil
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077342
- Marketed since
- December 11, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Sildenafil Citrate 100 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71205-088-10 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-088-10) | Aug 1, 2018 |
| 71205-088-20 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-088-20) | Apr 21, 2021 |
| 71205-088-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-088-30) | Aug 1, 2018 |
| 71205-088-50 | 50 TABLET, FILM COATED in 1 BOTTLE (71205-088-50) | Aug 1, 2018 |
| 71205-088-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-088-60) | Aug 1, 2018 |
| 71205-088-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-088-90) | Aug 1, 2018 |
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