Sildenafil
- Product NDC
- 50436-0711
- 11-digit product format
- 504360711
- Labeler code
- 50436
- Product ID
- 50436-0711_b4899bcd-ac95-433e-84ec-c49044e84a25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sildenafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA202659
- Marketing category
- ANDA
- Marketing start
- 2018-06-11
- Marketing end
- 0000-00-00
- Substance
- SILDENAFIL CITRATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0711-1 | Sildenafil | 1 in 1 POUCH | TABLET, FILM COATED | 1 | | 3 |
| 50436-0711-1 | Sildenafil | 1080 in 1 CASE | TABLET, FILM COATED | 1080 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0711 | SILDENAFIL TABLET, FILM COATED [UNIT DOSE SERVICES] | 3 | Legacy NDC, 2 package rows | 20191025_ce273b80-0509-4853-bd6d-2b64c0a53ef8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0711-1 | 50436071101 | 1 in 1 POUCH | Historical |