Metformin Hydrochloride
- Product NDC
- 67296-0700
- 11-digit product format
- 672960700
- Labeler code
- 67296
- Product ID
- 67296-0700_d5fc29b0-59c4-495f-e053-2995a90a1b6c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA077095
- Marketing category
- ANDA
- Marketing start
- 2005-01-14
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 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 |
|---|
| 67296-0700-1 | Metformin Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 4 |
| 67296-0700-3 | Metformin Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0700 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 2 package rows | 20220120_415c945b-6c6e-2a55-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 |
|---|
| 67296-0700-1 | 67296070001 | 60 TABLET, FILM COATED in 1 BOTTLE (67296-0700-1) | 2005-01-14 | 0000-00-00 | No | No | Current |
| 67296-0700-3 | 67296070003 | 30 TABLET, FILM COATED in 1 BOTTLE (67296-0700-3) | 2005-01-14 | 0000-00-00 | No | No | Current |