METFORMIN HYDROCHLORIDE
- Product NDC
- 55700-736
- 11-digit product format
- 557000736
- Labeler code
- 55700
- Product ID
- 55700-736_940e64b0-3fb4-438c-9413-fd348611ec20
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA203769
- Marketing category
- ANDA
- Marketing start
- 2019-03-29
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-736-30 | 55700073630 | 30 TABLET in 1 BOTTLE, PLASTIC (55700-736-30) | 30 tablet | 2020-03-17 | 0000-00-00 | No | No | Current |
| 55700-736-60 | 55700073660 | 60 TABLET in 1 BOTTLE, PLASTIC (55700-736-60) | 60 tablet | 2019-05-13 | 0000-00-00 | No | No | Current |
| 55700-736-90 | 55700073690 | 90 TABLET in 1 BOTTLE, PLASTIC (55700-736-90) | 90 tablet | 2019-03-29 | 0000-00-00 | No | No | Current |