Sildenafil Citrate
- Product NDC
- 71205-623
- 11-digit product format
- 712050623
- Labeler code
- 71205
- Product ID
- 71205-623_ad418ee5-a646-4d79-b10b-c7f3051f2977
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA204883
- Marketing category
- ANDA
- Marketing start
- 2016-08-01
- Substance
- SILDENAFIL CITRATE
- Active strength
- 20 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 |
|---|
| 71205-623-10 | 71205062310 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-623-10) | 2021-12-29 | No | No | Historical |
| 71205-623-30 | 71205062330 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-623-30) | 2021-11-23 | No | No | Historical |
| 71205-623-60 | 71205062360 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-623-60) | 2021-11-23 | No | No | Historical |
| 71205-623-90 | 71205062390 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-623-90) | 2021-11-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sildenafil Citrate | Proficient Rx LP | 2024-01-01 | HUMAN PRESCRIPTION DRUG LABEL | 4 |