Metoprolol Tartrate
- Product NDC
- 68788-9686
- 11-digit product format
- 687889686
- Labeler code
- 68788
- Product ID
- 68788-9686_d0eb19fd-5001-4860-a88e-cb0829f1376a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078459
- Marketing category
- ANDA
- Marketing start
- 2013-04-01
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record