METFORMIN HYDROCHLORIDE
- Product NDC
- 71455-104
- 11-digit product format
- 714550104
- Labeler code
- 71455
- Product ID
- 71455-104_a7999fa7-8870-33c7-e053-2995a90aa3f5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- UNYTER ENTERPRISES
- Application
- ANDA077095
- Marketing category
- ANDA
- Marketing start
- 2011-01-27
- 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 |
|---|
| 71455-104-00 | METFORMIN HYDROCHLORIDE | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71455-104 | METFORMIN HYDROCHLORIDE TABLET, FILM COATED [UNYTER ENTERPRISES] | 1 | Legacy NDC, 1 package rows | 20200714_a7999fa7-886f-33c7-e053-2995a90aa3f5.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 |
|---|
| 71455-104-00 | 71455010400 | 1000 TABLET, FILM COATED in 1 BOTTLE (71455-104-00) | 2011-01-27 | 0000-00-00 | No | No | Current |