Package 71610-502-53

Brand: benztropine mesylate

Generic: benztropine mesylate
NDC Package

Package Facts

Identity

Package NDC 71610-502-53
Digits Only 7161050253
Product NDC 71610-502
Description

60 TABLET in 1 BOTTLE (71610-502-53)

Marketing

Marketing Status
Marketed Since 2020-12-08
Brand benztropine mesylate
Generic benztropine mesylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "83880a96-336b-4e03-ac29-a41e62d78f3c", "openfda": {"unii": ["WMJ8TL7510"], "rxcui": ["885213"], "spl_set_id": ["f82c6455-f36b-49d7-881e-6601d513d846"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71610-502-53)", "package_ndc": "71610-502-53", "marketing_start_date": "20201208"}], "brand_name": "BENZTROPINE MESYLATE", "product_id": "71610-502_83880a96-336b-4e03-ac29-a41e62d78f3c", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Antihistamine [EPC]", "Cholinergic Antagonists [MoA]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "71610-502", "generic_name": "BENZTROPINE MESYLATE", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BENZTROPINE MESYLATE", "active_ingredients": [{"name": "BENZTROPINE MESYLATE", "strength": "1 mg/1"}], "application_number": "ANDA090168", "marketing_category": "ANDA", "marketing_start_date": "20121128", "listing_expiration_date": "20261231"}