METFORMIN HYDROCHLORIDE
- Product NDC
- 67296-1527
- 11-digit product format
- 672961527
- Labeler code
- 67296
- Product ID
- 67296-1527_d61fa317-4148-e321-e053-2a95a90ac5e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA077336
- Marketing category
- ANDA
- Marketing start
- 2006-02-09
- 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
- 2023-12-31
- 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 |
|---|
| 67296-1527-3 | METFORMIN HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1527 | METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 1 package rows | 20220123_56cfd673-6594-5292-e054-00144ff8d46c.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 |
|---|
| 67296-1527-3 | 67296152703 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-1527-3) | 2006-02-09 | 0000-00-00 | No | No | Current |