Ursodiol
- Product NDC
- 72162-1501
- 11-digit product format
- 721621501
- Labeler code
- 72162
- Product ID
- 72162-1501_ef4f0687-2fd1-43b2-9c55-e678cadb53d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ursodiol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202540
- Marketing category
- ANDA
- Marketing start
- 2013-08-01
- Substance
- URSODIOL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Bile Acid [EPC], Bile Acids and Salts [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ursodiol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| URSODIOL | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 724L30Y2QR |
| Rxcui | 858733 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1501-1 | Ursodiol | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 104 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1501 | URSODIOL TABLET, FILM COATED [BRYANT RANCH PREPACK] | 104 | Current NDC, 1 package rows | 20241013_be811c61-5f48-4b03-94b6-e6941b595621.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1501-1 | 72162150101 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-1501-1) | 2023-03-30 | No | No | Historical |