Sildenafil Citrate
- Product NDC
- 70934-435
- 11-digit product format
- 709340435
- Labeler code
- 70934
- Product ID
- 70934-435_acc7fea7-31b6-66ac-e053-2995a90a4946
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA204883
- Marketing category
- ANDA
- Marketing start
- 2019-09-03
- 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
- 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 |
|---|
| 70934-435-20 | 70934043520 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-435-20) | 2019-09-03 | 0000-00-00 | No | No | Current |