Tadalafil
- Product NDC
- 50090-6150
- 11-digit product format
- 500906150
- Labeler code
- 50090
- Product ID
- 50090-6150_bb96d614-7c9d-4d67-b6db-56f1ff64d9da
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tadalafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209167
- Marketing category
- ANDA
- Marketing start
- 2019-03-27
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6150 | TADALAFIL TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 4 | Legacy NDC | 20240110_a6847ad6-3b5b-47e5-a3b5-04dc3182d72b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-6150-0 | 50090615000 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-6150-0) | 2022-10-05 | 0000-00-00 | No | No | Current |
| 50090-6150-1 | 50090615001 | 10 TABLET, FILM COATED in 1 BOTTLE (50090-6150-1) | 2022-10-05 | 0000-00-00 | No | No | Current |