Sildenafil
- Product NDC
- 68071-2217
- 11-digit product format
- 680712217
- Labeler code
- 68071
- Product ID
- 68071-2217_d60baefd-283b-2417-e053-2a95a90a156d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA203623
- Marketing category
- ANDA
- Marketing start
- 2014-11-26
- 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
- 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 |
|---|
| 68071-2217-4 | 68071221704 | 4 TABLET, FILM COATED in 1 BOTTLE (68071-2217-4) | 2020-07-15 | 0000-00-00 | No | No | Current |