Sildenafil
- Product NDC
- 63629-8129
- 11-digit product format
- 636298129
- Labeler code
- 63629
- Product ID
- 63629-8129_5aeb77ec-359c-493e-bf14-de4f205c2d7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203814
- Marketing category
- ANDA
- Marketing start
- 2014-01-03
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- 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 |
|---|
| 63629-8129-1 | 63629812901 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8129-1) | 2019-07-29 | 0000-00-00 | No | No | Current |
| 63629-8129-2 | 63629812902 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-8129-2) | 2019-07-29 | 0000-00-00 | No | No | Current |