SILDENAFIL CITRATE
- Product NDC
- 43063-941
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SILDENAFIL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA091448
- Marketing category
- ANDA
- Substance
- SILDENAFIL CITRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 43063-941-15 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-941-15) | 20190130 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 78c4551c-b922-43c9-9a5a-66377ea07bc2 | These highlights do not include all the information needed to use SILDENAFIL TABLETS safely and effectively. See full prescribing information for SILDENAFIL TABLETS. SILDENAFIL tablets, for oral use Initial U.S. Approval:1998 | PD-Rx Pharmaceuticals, Inc. | 2026-05-27 | HUMAN PRESCRIPTION DRUG LABEL | 24 |