Metoprolol Succinate
- Product NDC
- 63739-454
- 11-digit product format
- 637390454
- Labeler code
- 63739
- Product ID
- 63739-454_0a4bd7da-8dcc-4f6c-bf4f-8f0dd6b593b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA077298
- Marketing category
- ANDA
- Marketing start
- 2010-04-15
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 100 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
FDA-Initiated Inactive NDC Indexing#