Metoprolol Tartrate
- Product NDC
- 68788-8932
- 11-digit product format
- 687888932
- Labeler code
- 68788
- Product ID
- 68788-8932_ebf46c26-c35f-4abd-a856-781e5eda19fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA074644
- Marketing category
- ANDA
- Marketing start
- 1997-07-01
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 50 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