Tadalafil
- Product NDC
- 70518-2972
- 11-digit product format
- 705182972
- Labeler code
- 70518
- Product ID
- 70518-2972_d7ace75a-765f-7b03-e053-2a95a90abb93
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tadalafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209167
- Marketing category
- ANDA
- Marketing start
- 2020-12-16
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2972-0 | 70518297200 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2972-0) | 2020-12-16 | 0000-00-00 | No | No | Current |