Metformin Hydrochloride
- Product NDC
- 70518-2920
- 11-digit product format
- 705182920
- Labeler code
- 70518
- Product ID
- 70518-2920_d79a45ce-b7de-8ac7-e053-2a95a90a33a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077078
- Marketing category
- ANDA
- Marketing start
- 2020-10-26
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 750 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2920 | METFORMIN HYDROCHLORIDE TABLET [REMEDYREPACK INC.] | 3 | Legacy NDC | 20220210_4b081178-8826-4c27-8354-4904a52821b1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2920-0 | 70518292000 | 30 TABLET in 1 BLISTER PACK (70518-2920-0) | 30 tablet | 2020-10-26 | 0000-00-00 | No | No | Current |