Metoprolol Tartrate
- Product NDC
- 68788-9890
- 11-digit product format
- 687889890
- Labeler code
- 68788
- Product ID
- 68788-9890_45c84855-0e91-4660-9350-4250bf6a3e5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA074644
- Marketing category
- ANDA
- Marketing start
- 2012-02-14
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record