METFORMIN HYDROCHLORIDE
- Product NDC
- 67877-932
- 11-digit product format
- 678770932
- Labeler code
- 67877
- Product ID
- 67877-932_8c7835fa-3f68-4850-b1da-34893bafb485
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Ascend Laboratories, LLC
- Application
- ANDA213320
- Marketing category
- ANDA
- Marketing start
- 2025-08-25
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 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 | 1000 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 786Z46389E |
| Rxcui | 861004, 861007, 861010 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67877-932-01 | METFORMIN HYDROCHLORIDE | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 1 |
| 67877-932-05 | METFORMIN HYDROCHLORIDE | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 1 |
| 67877-932-10 | METFORMIN HYDROCHLORIDE | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 67877-932-01 | 67877093201 | 100 TABLET, FILM COATED in 1 BOTTLE (67877-932-01) | 2025-08-25 | No | No | Historical |
| 67877-932-05 | 67877093205 | 500 TABLET, FILM COATED in 1 BOTTLE (67877-932-05) | 2025-08-25 | No | No | Historical |
| 67877-932-10 | 67877093210 | 1000 TABLET, FILM COATED in 1 BOTTLE (67877-932-10) | 2025-08-25 | No | No | Historical |