Sildenafil Citrate
- Product NDC
- 68071-3631
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA206401
- Marketing category
- ANDA
- Substance
- SILDENAFIL CITRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3631-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3631-3) | 2024-06-17 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sildenafil Citrate | NuCare Pharmaceuticals,Inc. | 2024-06-17 | HUMAN PRESCRIPTION DRUG LABEL | 1 |