Chenodiol
- Product NDC
- 0722-7121
- 11-digit product format
- 007227121
- Labeler code
- 0722
- Product ID
- 0722-7121_ff0d39d3-8c53-4d01-b4b6-5d39c1b50af4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chenodiol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Nexgen Pharma, Inc.
- Application
- ANDA091019
- Marketing category
- ANDA
- Marketing start
- 2009-10-22
- Marketing end
- 0000-00-00
- Substance
- CHENODIOL
- Active strength
- 250 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 0722-7121-01 | Chenodiol | 1 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 1 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0722-7121 | CHENODIOL TABLET, FILM COATED [NEXGEN PHARMA, INC.] | 5 | Legacy NDC, 1 package rows | 20190907_bbb86251-9423-40e6-9117-9511ab5fbf63.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 0722-7121-01 | 00722712101 | 1 in 1 BOTTLE, PLASTIC | Historical |