SILDENAFIL CITRATE
- Product NDC
- 71205-795
- 11-digit product format
- 712050795
- Labeler code
- 71205
- Product ID
- 71205-795_6fd94b93-d76c-43d0-a1cc-85fef542960e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SILDENAFIL CITRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA209302
- Marketing category
- ANDA
- Marketing start
- 2020-09-04
- Substance
- SILDENAFIL CITRATE
- Active strength
- 50 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 |
|---|
| 71205-795-10 | 71205079510 | 10 TABLET in 1 BOTTLE (71205-795-10) | 10 tablet | 2023-04-20 | No | No | Historical |
| 71205-795-11 | 71205079511 | 1000 TABLET in 1 BOTTLE (71205-795-11) | 1000 tablet | 2025-10-30 | No | No | Historical |
| 71205-795-20 | 71205079520 | 20 TABLET in 1 BOTTLE (71205-795-20) | 20 tablet | 2023-04-20 | No | No | Historical |
| 71205-795-30 | 71205079530 | 30 TABLET in 1 BOTTLE (71205-795-30) | 30 tablet | 2023-04-20 | No | No | Historical |
| 71205-795-60 | 71205079560 | 60 TABLET in 1 BOTTLE (71205-795-60) | 60 tablet | 2023-04-20 | No | No | Historical |
| 71205-795-90 | 71205079590 | 90 TABLET in 1 BOTTLE (71205-795-90) | 90 tablet | 2023-04-20 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| SILDENAFIL CITRATE | Proficient Rx LP | 2025-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |
| SILDENAFIL CITRATE | Proficient Rx LP | 2023-04-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |