tadalafil
- Product NDC
- 72789-430
- 11-digit product format
- 727890430
- Labeler code
- 72789
- Product ID
- 72789-430_4124275a-656a-c603-e063-6294a90ab68f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tadalafil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA215556
- Marketing category
- ANDA
- Marketing start
- 2023-04-01
- Substance
- TADALAFIL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- tadalafil
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TADALAFIL | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 742SXX0ICT |
| Rxcui | 484814 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-430-90 | tadalafil | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-430 | TADALAFIL TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.] | 4 | Current NDC, 1 package rows | 20240918_6c680b37-d515-4fc2-83e6-411f1017e18c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-430-90 | 72789043090 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-430-90) | 2024-09-16 | No | No | Current |