Sildenafil
- Product NDC
- 48792-7911
- 11-digit product format
- 487927911
- Labeler code
- 48792
- Product ID
- 48792-7911_a8a33461-e732-e4a9-e053-2995a90a42bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sunshine Lake Pharma Co., Ltd
- Application
- ANDA213032
- Marketing category
- ANDA
- Marketing start
- 2020-06-11
- Marketing end
- 0000-00-00
- Substance
- SILDENAFIL CITRATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 48792-7911-1 | 48792791101 | 30 TABLET, FILM COATED in 1 BOTTLE (48792-7911-1) | 2020-06-11 | 0000-00-00 | No | No | Current |