METFORMIN HYDROCHLORIDE
- Product NDC
- 61919-922
- 11-digit product format
- 619190922
- Labeler code
- 61919
- Product ID
- 61919-922_9c98b843-f92c-458f-e053-2a95a90ab435
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA090295
- Marketing category
- ANDA
- Marketing start
- 2018-03-13
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-922-60 | METFORMIN HYDROCHLORIDE | 60 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-922 | METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE [DIRECT RX] | 2 | Legacy NDC, 1 package rows | 20200121_674bf07f-8123-1204-e053-2991aa0a73b4.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 |
|---|
| 61919-922-60 | 61919092260 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-922-60) | 2018-03-13 | 0000-00-00 | No | No | Current |