Sildenafil
- Product NDC
- 70859-015
- 11-digit product format
- 708590015
- Labeler code
- 70859
- Product ID
- 70859-015_c18301c4-e134-543b-e053-2a95a90ac13e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA203814
- Marketing category
- ANDA
- Marketing start
- 2014-01-03
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70859-015-28 | 70859001528 | 28 TABLET, FILM COATED in 1 BOTTLE (70859-015-28) | 2017-05-11 | 0000-00-00 | No | No | Current |