SILDENAFIL CITRATE
- Product NDC
- 82804-251
- 11-digit product format
- 828040251
- Labeler code
- 82804
- Product ID
- 82804-251_1add0cab-8873-4cd1-ab53-e05c4ac458b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SILDENAFIL CITRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA209302
- Marketing category
- ANDA
- Marketing start
- 2021-06-16
- Substance
- SILDENAFIL CITRATE
- Active strength
- 25 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 |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-251-11 | 82804025111 | 1000 TABLET in 1 BOTTLE (82804-251-11) | 1000 tablet | 2025-10-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| SILDENAFIL CITRATE | Proficient Rx LP | 2025-10-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |