Metformin Hydrochloride
- Product NDC
- 50436-0700
- 11-digit product format
- 504360700
- Labeler code
- 50436
- Product ID
- 50436-0700_cb08a6a0-686b-408e-902e-bdb8152b3c0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA078321
- Marketing category
- ANDA
- Marketing start
- 2008-04-17
- 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
- 2020-12-31
- 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 |
|---|
| 50436-0700-3 | Metformin Hydrochloride | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0700 | METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE [UNIT DOSE SERVICES] | 2 | Legacy NDC, 1 package rows | 20181010_a9dd42c0-8f4a-4254-a1bd-9c298060cb98.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0700-3 | 50436070003 | 90 in 1 BOTTLE | Historical |