Metformin Hydrochloride
- Product NDC
- 68071-2316
- 11-digit product format
- 680712316
- Labeler code
- 68071
- Product ID
- 68071-2316_d58ecefc-cc0a-682e-e053-2a95a90a35ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA209882
- Marketing category
- ANDA
- Marketing start
- 2019-01-15
- 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 |
|---|
| 68071-2316-6 | Metformin Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2316 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 2 | Legacy NDC, 1 package rows | 20220115_b6ac1965-c757-e474-e053-2a95a90a6e47.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 |
|---|
| 68071-2316-6 | 68071231606 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-2316-6) | 2020-12-17 | 0000-00-00 | No | No | Current |