Sildenafil
- Product NDC
- 68071-3832
- 11-digit product format
- 680713832
- Labeler code
- 68071
- Product ID
- 68071-3832_3314cf58-b7ab-c69f-e063-6294a90aab33
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA203962
- Marketing category
- ANDA
- Marketing start
- 2018-06-11
- Substance
- SILDENAFIL CITRATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| BW9B0ZE037 | SILDENAFIL CITRATE | 171599-83-0 | SILDENAFIL CITRATE |
| 3M7OB98Y7H | SILDENAFIL | 139755-83-2 | Sildenafil |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3832-3 | 68071383203 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3832-3) | 2025-04-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sildenafil | NuCare Pharmaceuticals, Inc. | 2025-04-18 | HUMAN PRESCRIPTION DRUG LABEL | 1 |