Sildenafil for Oral Suspension
- Product NDC
- 69097-903
- 11-digit product format
- 690970903
- Labeler code
- 69097
- Product ID
- 69097-903_1baf8602-87b5-46e9-b8c7-bfc88b535f0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sildenafil citrate
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Cipla USA Inc.
- Application
- ANDA213041
- Marketing category
- ANDA
- Marketing start
- 2021-08-18
- Marketing end
- 0000-00-00
- Substance
- SILDENAFIL CITRATE
- Active strength
- 10 mg/mL
- 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69097-903-44 | 69097090344 | 1 BOTTLE in 1 CARTON (69097-903-44) > 112 mL in 1 BOTTLE | 1 bottle | 2021-08-18 | 0000-00-00 | No | No | Current |