Tadalafil
- Product NDC
- 71335-1334
- 11-digit product format
- 713351334
- Labeler code
- 71335
- Product ID
- 71335-1334_e1c4f116-c21a-4686-b59c-29324986e57e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tadalafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209908
- Marketing category
- ANDA
- Marketing start
- 2019-03-26
- Marketing end
- 0000-00-00
- Substance
- TADALAFIL
- Active strength
- 10 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 |
|---|
| 71335-1334-1 | 71335133401 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1334-1) | 2019-03-26 | 0000-00-00 | No | No | Current |
| 71335-1334-2 | 71335133402 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1334-2) | 2019-03-26 | 0000-00-00 | No | No | Current |
| 71335-1334-3 | 71335133403 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1334-3) | 2019-03-26 | 0000-00-00 | No | No | Current |
| 71335-1334-4 | 71335133404 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1334-4) | 2019-03-26 | 0000-00-00 | No | No | Current |