Sildenafil
- Product NDC
- 70934-472
- 11-digit product format
- 709340472
- Labeler code
- 70934
- Product ID
- 70934-472_b7ae78b1-a5bb-2d0f-e053-2995a90ae1f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA202659
- Marketing category
- ANDA
- Marketing start
- 2019-12-05
- Marketing end
- 0000-00-00
- Substance
- SILDENAFIL CITRATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70934-472-06 | 70934047206 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-472-06) | 2019-12-05 | 0000-00-00 | No | No | Current |
| 70934-472-15 | 70934047215 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-472-15) | 2019-12-05 | 0000-00-00 | No | No | Current |