Metformin hydrochloride
- Product NDC
- 27241-189
- 11-digit product format
- 272410189
- Labeler code
- 27241
- Product ID
- 27241-189_43afafd3-86ce-4aaa-8442-42f6ee5ab488
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Ajanta Pharma USA Inc.
- Application
- ANDA213651
- Marketing category
- ANDA
- Marketing start
- 2020-04-09
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metformin hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METFORMIN HYDROCHLORIDE | 1000 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 786Z46389E |
| Rxcui | 1807894, 1807917 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 27241-189-60 | Metformin hydrochloride | 60 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 60 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 27241-189 | METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE [AJANTA PHARMA USA INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20211124_6d9179a8-9579-4804-a4c7-633f37aef1ee.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 |
|---|
| 27241-189-60 | 27241018960 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-189-60) | 2020-04-09 | 0000-00-00 | No | No | Current |