Metoprolol Tartrate
- Product NDC
- 55700-674
- 11-digit product format
- 557000674
- Labeler code
- 55700
- Product ID
- 55700-674_a8419699-7ea4-45aa-9d17-7df70630aad3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA200981
- Marketing category
- ANDA
- Marketing start
- 2018-08-31
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record