Tadalafil
- Product NDC
- 50436-6440
- 11-digit product format
- 504366440
- Labeler code
- 50436
- Product ID
- 50436-6440_a82b4311-f35e-49da-a9d4-ac63d350d5aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tadalafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA209908
- 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 |
|---|
| 50436-6440-1 | Tadalafil | 1890 in 1 CASE | TABLET, FILM COATED | 1890 | | 2 |
| 50436-6440-1 | Tadalafil | 1 in 1 POUCH | TABLET, FILM COATED | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-6440 | TADALAFIL TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | Legacy NDC, 2 package rows | 20191025_bb4a77aa-f18e-4c53-9b70-70f402ba6b12.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-6440-1 | 50436644001 | 1890 in 1 CASE | Historical |