Metformin hydrochloride
- Product NDC
- 24724-014
- 11-digit product format
- 247240014
- Labeler code
- 24724
- Product ID
- 24724-014_7ba4b972-10a4-43d3-9b5f-ec4915db9d88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- INDICUS PHARMA LLC
- Application
- ANDA079148
- Marketing category
- ANDA
- Marketing start
- 2009-06-03
- 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 |
|---|
| 24724-014-01 | Metformin hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 5 |
| 24724-014-50 | Metformin hydrochloride | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24724-014 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED [INDICUS PHARMA LLC] | 5 | Legacy NDC, 2 package rows | 20201204_56d13a1c-b289-4528-b23c-60f5427b4552.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 |
|---|
| 24724-014-01 | 24724001401 | 100 TABLET, FILM COATED in 1 BOTTLE (24724-014-01) | 2009-06-03 | 0000-00-00 | No | No | Current |
| 24724-014-50 | 24724001450 | 500 TABLET, FILM COATED in 1 BOTTLE (24724-014-50) | 2009-06-03 | 0000-00-00 | No | No | Current |