Sildenafil
- Product NDC
- 70934-849
- 11-digit product format
- 709340849
- Labeler code
- 70934
- Product ID
- 70934-849_c0a83060-4a99-02e0-e053-2a95a90a5445
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sildinafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA201150
- Marketing category
- ANDA
- Marketing start
- 2021-03-29
- 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 |
|---|
| 70934-849-20 | 70934084920 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-849-20) | 2021-04-23 | 0000-00-00 | No | No | Current |
| 70934-849-30 | 70934084930 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-849-30) | 2021-03-29 | 0000-00-00 | No | No | Current |