VARDENAFIL
- Product NDC
- 51407-174
- 11-digit product format
- 514070174
- Labeler code
- 51407
- Product ID
- 51407-174_efcefe93-0ec7-2aa1-e053-2995a90a8f22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VARDENAFIL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA208960
- Marketing category
- ANDA
- Marketing start
- 2018-10-31
- Marketing end
- 0000-00-00
- Substance
- VARDENAFIL HYDROCHLORIDE TRIHYDRATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-174-30 | 51407017430 | 30 TABLET, FILM COATED in 1 BOTTLE (51407-174-30) | 2021-07-29 | 0000-00-00 | No | No | Current |