Metoprolol tartrate
- Product NDC
- 50436-6579
- 11-digit product format
- 504366579
- Labeler code
- 50436
- Product ID
- 50436-6579_a5f04fd8-d4d3-4cd2-b5a9-e93438b32faf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA074644
- Marketing category
- ANDA
- Marketing start
- 2015-06-29
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 100 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