Sildenafil
- Product NDC
- 68788-7680
- 11-digit product format
- 687887680
- Labeler code
- 68788
- Product ID
- 68788-7680_97447e02-023e-4de8-9b35-cdb36d24e190
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA203623
- Marketing category
- ANDA
- Marketing start
- 2020-03-02
- 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 |
|---|
| 68788-7680-1 | 68788768001 | 10 TABLET, FILM COATED in 1 BOTTLE (68788-7680-1) | 2021-09-14 | 0000-00-00 | No | No | Current |
| 68788-7680-3 | 68788768003 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7680-3) | 2020-03-02 | 0000-00-00 | No | No | Current |
| 68788-7680-4 | 68788768004 | 4 TABLET, FILM COATED in 1 BOTTLE (68788-7680-4) | 2020-03-02 | 0000-00-00 | No | No | Current |
| 68788-7680-6 | 68788768006 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7680-6) | 2020-03-02 | 0000-00-00 | No | No | Current |
| 68788-7680-7 | 68788768007 | 7 TABLET, FILM COATED in 1 BOTTLE (68788-7680-7) | 2021-09-14 | 0000-00-00 | No | No | Current |
| 68788-7680-9 | 68788768009 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7680-9) | 2020-03-02 | 0000-00-00 | No | No | Current |