Tadalafil
- Product NDC
- 70518-3529
- 11-digit product format
- 705183529
- Labeler code
- 70518
- Product ID
- 70518-3529_f111dc50-52e0-7210-e053-2995a90a1b96
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tadalafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207290
- Marketing category
- ANDA
- Marketing start
- 2020-09-20
- Marketing end
- 0000-00-00
- Substance
- TADALAFIL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-3529-0 | 70518352900 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3529-0) | 2020-09-20 | 0000-00-00 | No | No | Current |