Tadalafil
- Product NDC
- 0378-6976
- 11-digit product format
- 003786976
- Labeler code
- 0378
- Product ID
- 0378-6976_bb3aae41-95dc-4c00-966a-5c961292ef12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tadalafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA200630
- Marketing category
- ANDA
- Marketing start
- 2019-03-01
- Marketing end
- 2021-09-30
- Substance
- TADALAFIL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0378-6976-91 | 00378697691 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6976-91) | 2019-03-01 | 0000-00-00 | No | No | Current |