Sildenafil
- Product NDC
- 72162-2363
- 11-digit product format
- 721622363
- Labeler code
- 72162
- Product ID
- 72162-2363_1cf7d6c3-6e03-41e9-a3fd-41ef724ec69c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203623
- Marketing category
- ANDA
- Marketing start
- 2014-11-26
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sildenafil
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SILDENAFIL CITRATE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | BW9B0ZE037 |
| Rxcui | 577033 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2363-9 | Sildenafil | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2363 | SILDENAFIL (SILDENAFIL) TABLET, FILM COATED [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20241122_591a4ae7-e06c-42b6-85af-f03fd2fb8959.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2363-9 | 72162236309 | 90 TABLET, FILM COATED in 1 BOTTLE (72162-2363-9) | 2024-07-16 | No | No | Historical |