NDC 71335-1005 – Sildenafil
Sildenafil Citrate 20 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1005
Product details
- Brand name
- Sildenafil
- Generic name
- Sildenafil
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203814
- Marketed since
- January 3, 2014
- Marketing end
- October 31, 2027
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Sildenafil Citrate 20 mg/1
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1005-1 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1005-1) | Oct 14, 2016 |
| 71335-1005-2 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1005-2) | Oct 14, 2016 |
| 71335-1005-3 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-1005-3) | Oct 14, 2016 |
| 71335-1005-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1005-4) | Oct 14, 2016 |
| 71335-1005-5 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1005-5) | Oct 14, 2016 |
| 71335-1005-6 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1005-6) | Oct 14, 2016 |
| 71335-1005-7 | 270 TABLET, FILM COATED in 1 BOTTLE (71335-1005-7) | Oct 14, 2016 |
| 71335-1005-8 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-1005-8) | Oct 14, 2016 |
| 71335-1005-9 | 12 TABLET, FILM COATED in 1 BOTTLE (71335-1005-9) | Oct 14, 2016 |
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