Sildenafil
- Product NDC
- 71610-256
- 11-digit product format
- 716100256
- Labeler code
- 71610
- Product ID
- 71610-256_7ef34ca8-1a02-40a3-83a4-4b1dcf3a93d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- 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
- 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 |
|---|
| 71610-256-02 | 71610025602 | 2 TABLET, FILM COATED in 1 BOTTLE (71610-256-02) | 2019-03-29 | 0000-00-00 | No | No | Current |
| 71610-256-04 | 71610025604 | 4 TABLET, FILM COATED in 1 BOTTLE (71610-256-04) | 2019-03-29 | 0000-00-00 | No | No | Current |
| 71610-256-06 | 71610025606 | 6 TABLET, FILM COATED in 1 BOTTLE (71610-256-06) | 2019-03-29 | 0000-00-00 | No | No | Current |
| 71610-256-12 | 71610025612 | 12 TABLET, FILM COATED in 1 BOTTLE (71610-256-12) | 2019-03-29 | 0000-00-00 | No | No | Current |