BENZTROPINE MESYLATE
- Product NDC
- 71335-0382
- 11-digit product format
- 713350382
- Labeler code
- 71335
- Product ID
- 71335-0382_06f2d4bf-d9a5-4701-98f9-f52d9ea27be3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENZTROPINE MESYLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090168
- Marketing category
- ANDA
- Marketing start
- 2012-11-28
- Marketing end
- 0000-00-00
- Substance
- BENZTROPINE MESYLATE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record