Vardenafil Hydrochloride
- Product NDC
- 72162-2236
- 11-digit product format
- 721622236
- Labeler code
- 72162
- Product ID
- 72162-2236_891c56c9-912d-4e77-8649-c130c93424d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vardenafil Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209057
- Marketing category
- ANDA
- Marketing start
- 2018-11-01
- Substance
- VARDENAFIL HYDROCHLORIDE
- 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 |
|---|
| 5M8S2CU0TS | VARDENAFIL HYDROCHLORIDE | 330808-88-3 | VARDENAFIL HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2236-3 | 72162223603 | 30 TABLET in 1 BOTTLE (72162-2236-3) | 30 tablet | 2024-09-06 | No | No | Historical |