TADALAFIL
- Product NDC
- 68071-3601
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tadalafil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA210609
- Marketing category
- ANDA
- Substance
- TADALAFIL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3601-3 | 30 TABLET in 1 BOTTLE (68071-3601-3) | 2024-05-03 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| TADALAFIL | NuCare Pharmaceuticals,Inc. | 2024-05-03 | HUMAN PRESCRIPTION DRUG LABEL | 1 |