Sildenafil
- Product NDC
- 68071-1687
- 11-digit product format
- 680711687
- Labeler code
- 68071
- Product ID
- 68071-1687_5a1b1f78-42f4-31ed-e053-2a91aa0a2e1e
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record