Sildenafil
- Product NDC
- 51672-4231
- 11-digit product format
- 516724231
- Labeler code
- 51672
- Product ID
- 51672-4231_76034165-242b-48e5-8903-805f45e70e1e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SILDENAFIL CITRATE
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Taro Pharmaceuticals U.S.A. Inc.
- Application
- ANDA215522
- Marketing category
- ANDA
- Marketing start
- 2021-11-16
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51672-4231 | SILDENAFIL (SILDENAFIL CITRATE) POWDER, FOR SUSPENSION [TARO PHARMACEUTICALS U.S.A. INC.] | 7 | Legacy NDC | 20240509_e9c015d9-a70e-4781-b2d5-f89ce9d23c5a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51672-4231-8 | 51672423108 | 1 BOTTLE in 1 CARTON (51672-4231-8) > 112 mL in 1 BOTTLE | 1 bottle | 2021-11-16 | 0000-00-00 | No | No | Current |