Tadalafil
- Product NDC
- 60505-4683
- 11-digit product format
- 605054683
- Labeler code
- 60505
- Product ID
- 60505-4683_d051938b-170b-8a2b-e053-2995a90add3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tadalafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA210420
- Marketing category
- ANDA
- Marketing start
- 2019-03-26
- Marketing end
- 2022-02-28
- Substance
- TADALAFIL
- Active strength
- 3 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 |
|---|
| 60505-4683-3 | 60505468303 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-4683-3) | 2019-03-26 | 0000-00-00 | No | No | Current |