Tadalafil
- Product NDC
- 50436-1120
- 11-digit product format
- 504361120
- Labeler code
- 50436
- Product ID
- 50436-1120_68476ca8-79c8-450e-b123-5ce2760d2507
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tadalafil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA209654
- Marketing category
- ANDA
- Marketing start
- 2019-03-26
- Marketing end
- 0000-00-00
- Substance
- TADALAFIL
- Active strength
- 5 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 |
|---|
| 50436-1120-1 | Tadalafil | 1 in 1 POUCH | TABLET | 1 | | 3 |
| 50436-1120-1 | Tadalafil | 200 in 1 CASE | TABLET | 200 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-1120 | TADALAFIL TABLET [UNIT DOSE SERVICES] | 3 | Legacy NDC, 2 package rows | 20190905_c7654cb8-a46d-484a-a95f-59d5c4aa871f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-1120-1 | 50436112001 | 1 in 1 POUCH | Historical |