Metformin Hydrochloride
- Product NDC
- 70882-125
- 11-digit product format
- 708820125
- Labeler code
- 70882
- Product ID
- 70882-125_61b6dfd4-ea72-40f3-b4cd-0a51e8a810a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cambridge Therapeutics Technologies, LLC
- Application
- ANDA091184
- Marketing category
- ANDA
- Marketing start
- 2011-01-31
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 850 mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metformin Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METFORMIN HYDROCHLORIDE | 850 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 786Z46389E |
| Rxcui | 861010 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70882-125-30 | Metformin Hydrochloride | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70882-125 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED [CAMBRIDGE THERAPEUTICS TECHNOLOGIES, LLC] | 1 | Current NDC, Legacy NDC, 1 package rows | 20170608_9c333ae3-a4df-483b-9103-762134add15e.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 |
|---|
| 70882-125-30 | 70882012530 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70882-125-30) | 2011-01-31 | 0000-00-00 | No | No | Current |