Sildenafil
- Product NDC
- 50090-2618
- 11-digit product format
- 500902618
- Labeler code
- 50090
- Product ID
- 50090-2618_06d19ac1-1a3e-44eb-a85a-cca44297629b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078380
- Marketing category
- ANDA
- Marketing start
- 2013-05-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2618-0 | 50090261800 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-2618-0) | 2016-11-14 | 0000-00-00 | No | No | Current |
| 50090-2618-1 | 50090261801 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-2618-1) | 2016-11-14 | 0000-00-00 | No | No | Current |