Metoprolol Tartrate and Hydrochlorothiazide
- Product NDC
- 13811-671
- 11-digit product format
- 138110671
- Labeler code
- 13811
- Product ID
- 13811-671_18fe1a05-215b-445b-b309-580660325a43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Trigen Laboratories, LLC
- Application
- ANDA202870
- Marketing category
- ANDA
- Marketing start
- 2013-09-17
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE; HYDROCHLOROTHIAZIDE
- Active strength
- 100 mg/1; mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record