NDC 48433-326-01 - Metformin Hydrochloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 48433-326
- Requested NDC
- 48433-326-01
- Package NDCs from labels
- 48433-326-01, 48433-326-10
- Manufacturer
- Safecor Health, LLC
- Effective date
- 2013-09-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Metformin Hydrochloride - Safecor Health, LLC | Safecor Health, LLC | 2013-09-06 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 48433-326-10 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-153c-f424-e053-dadaa90a57ce | METFORMIN HYDROCHLORIDE TABLETS USP, 500 mg Rx only |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48433-326-01 | Metformin Hydrochloride | 1 in 1 POUCH | TABLET, FILM COATED | 1 | 1 | |
| 48433-326-10 | Metformin Hydrochloride | 100 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 100 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.