Tadalafil
- Product NDC
- 66993-703
- 11-digit product format
- 669930703
- Labeler code
- 66993
- Product ID
- 66993-703_2d8ed1c6-d14c-4d1e-852e-d7015d439146
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tadalafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Application
- NDA021368
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2018-09-27
- 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
- 2021-12-31
- 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 |
|---|
| 66993-703-30 | 66993070330 | 30 TABLET, FILM COATED in 1 BOTTLE (66993-703-30) | 2018-09-27 | 0000-00-00 | No | No | Current |