METFORMIN HYDROCHLORIDE
- Product NDC
- 60760-523
- 11-digit product format
- 607600523
- Labeler code
- 60760
- Product ID
- 60760-523_ded43b3e-9705-4219-e053-2a95a90a73f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA203769
- Marketing category
- ANDA
- Marketing start
- 2021-12-28
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-523 | METFORMIN HYDROCHLORIDE TABLET [ST. MARY'S MEDICAL PARK PHARMACY] | 9 | Legacy NDC | 20220513_d7103922-2007-1eb4-e053-2995a90aad4e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-523-60 | 60760052360 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-523-60) | 60 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |