Sildenafil
- Product NDC
- 42291-747
- 11-digit product format
- 422910747
- Labeler code
- 42291
- Product ID
- 42291-747_e80922f4-a465-b8c4-e053-2a95a90af313
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA077342
- Marketing category
- ANDA
- Marketing start
- 2018-05-29
- Marketing end
- 0000-00-00
- Substance
- SILDENAFIL CITRATE
- Active strength
- 50 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 |
|---|
| 42291-747-01 | 42291074701 | 100 TABLET, FILM COATED in 1 BOTTLE (42291-747-01) | 2018-05-29 | 0000-00-00 | No | No | Current |
| 42291-747-02 | 42291074702 | 2 TABLET, FILM COATED in 1 BOTTLE (42291-747-02) | 2018-05-29 | 0000-00-00 | No | No | Current |
| 42291-747-06 | 42291074706 | 6 TABLET, FILM COATED in 1 BOTTLE (42291-747-06) | 2018-09-04 | 0000-00-00 | No | No | Current |
| 42291-747-30 | 42291074730 | 30 TABLET, FILM COATED in 1 BOTTLE (42291-747-30) | 2018-05-29 | 0000-00-00 | No | No | Current |