Tadalafil
- Product NDC
- 61919-889
- 11-digit product format
- 619190889
- Labeler code
- 61919
- Product ID
- 61919-889_8b34e71c-fb67-3edf-e053-2a95a90a40fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tadalafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA209908
- Marketing category
- ANDA
- Marketing start
- 2019-06-13
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-889-30 | 61919088930 | 30 TABLET, FILM COATED in 1 BOTTLE (61919-889-30) | 2019-06-13 | 0000-00-00 | No | No | Current |