Metoprolol Tartrate
- Product NDC
- 68071-4634
- 11-digit product format
- 680714634
- Labeler code
- 68071
- Product ID
- 68071-4634_7b1c99d6-3dea-0881-e053-2a91aa0a0ddc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077739
- Marketing category
- ANDA
- Marketing start
- 2007-09-11
- 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