Sildenafil
- Product NDC
- 50090-1766
- 11-digit product format
- 500901766
- Labeler code
- 50090
- Product ID
- 50090-1766_206e33ff-c083-4275-951f-060f1ef6eb4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202025
- Marketing category
- ANDA
- Marketing start
- 2012-11-08
- 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
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50090-1766-0 | 50090176600 | 30 TABLET in 1 BOTTLE (50090-1766-0) | 30 tablet | 2015-04-02 | 0000-00-00 | No | No | Current |
| 50090-1766-1 | 50090176601 | 90 TABLET in 1 BOTTLE (50090-1766-1) | 90 tablet | 2016-06-30 | 0000-00-00 | No | No | Current |