METFORMIN HYDROCHLORIDE
- Product NDC
- 67296-1643
- 11-digit product format
- 672961643
- Labeler code
- 67296
- Product ID
- 67296-1643_b8df8208-820f-72a9-e053-2a95a90ae5cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metformin hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA201991
- Marketing category
- ANDA
- Marketing start
- 2019-01-01
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 67296-1643-3 | METFORMIN HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | | 16 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1643 | METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE [REDPHARM DRUG, INC.] | 16 | Legacy NDC, 1 package rows | 20210115_88f1fd59-6906-9755-e053-2a95a90acc61.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1643-3 | 67296164303 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-1643-3) | 2019-01-01 | 0000-00-00 | No | No | Current |