Metoprolol Tartrate
- Product NDC
- 43063-846
- 11-digit product format
- 430630846
- Labeler code
- 43063
- Product ID
- 43063-846_84148213-3e32-4e78-e053-2a91aa0a589a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA200981
- Marketing category
- ANDA
- Marketing start
- 2015-08-14
- 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