Benztropine Mesylate
- Product NDC
- 14789-300
- 11-digit product format
- 147890300
- Labeler code
- 14789
- Product ID
- 14789-300_bbacbb05-2e18-4cf9-b239-6addb60b7533
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENZTROPINE MESYLATE
- Dosage form
- INJECTION
- Route
- PARENTERAL
- Labeler
- Nexus Pharmaceuticals Inc
- Application
- ANDA090233
- Marketing category
- ANDA
- Marketing start
- 2009-07-29
- Marketing end
- 0000-00-00
- Substance
- BENZTROPINE MESYLATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#