Metformin Hydrochloride
- Product NDC
- 51224-220
- 11-digit product format
- 512240220
- Labeler code
- 51224
- Product ID
- 51224-220_62d835b1-e8f8-439a-bfb1-d42a18c431bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- TAGI Pharma, Inc.
- Application
- ANDA205096
- Marketing category
- ANDA
- Marketing start
- 2019-05-01
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51224-220 | METFORMIN HYDROCHLORIDE TABLET, COATED [TAGI PHARMA, INC.] | 1 | Legacy NDC | 20190501_9e8686e9-cc6e-41a5-8709-215a6670575a.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 |
|---|
| 51224-220-50 | 51224022050 | 100 TABLET, COATED in 1 BOTTLE (51224-220-50) | 2019-05-01 | 0000-00-00 | No | No | Current |
| 51224-220-60 | 51224022060 | 500 TABLET, COATED in 1 BOTTLE (51224-220-60) | 2019-05-01 | 0000-00-00 | No | No | Current |
| 51224-220-70 | 51224022070 | 1000 TABLET, COATED in 1 BOTTLE (51224-220-70) | 2019-05-01 | 0000-00-00 | No | No | Current |