URUSA
- Product NDC
- 72689-0001
- 11-digit product format
- 726890001
- Labeler code
- 72689
- Product ID
- 72689-0001_7b0f3ea2-9553-392b-e053-2991aa0ad971
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ursodeoxycholic Acid
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- OASIS TRADING
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-11-15
- Marketing end
- 0000-00-00
- Substance
- URSODIOL
- Active strength
- 250 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72689-0001-1 | URUSA | 60 in 1 BLISTER PACK | CAPSULE | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72689-0001 | URUSA (URSODEOXYCHOLIC ACID) CAPSULE [OASIS TRADING] | 2 | Legacy NDC, 1 package rows | 20181120_7aa650ea-167b-cdd8-e053-2991aa0a7896.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 72689-0001-1 | 72689000101 | 60 in 1 BLISTER PACK | Historical |