Sildenafil Citrate
- Product NDC
- 50090-5906
- 11-digit product format
- 500905906
- Labeler code
- 50090
- Product ID
- 50090-5906_c4b0520b-1ae4-4da8-90de-e93016c34a76
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA206401
- Marketing category
- ANDA
- Marketing start
- 2018-10-12
- Substance
- SILDENAFIL CITRATE
- Active strength
- 25 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 Citrate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SILDENAFIL CITRATE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | BW9B0ZE037 |
| Rxcui | 314228 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-5906-0 | Sildenafil Citrate | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5906 | SILDENAFIL CITRATE (SILDENAFIL) TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231125_bf1a22a2-6a69-46c9-933d-e474e88637e9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5906-0 | 50090590600 | 10 TABLET, FILM COATED in 1 BOTTLE (50090-5906-0) | 2022-01-17 | 0000-00-00 | No | No | Current |