Package 49884-065-01

Brand: glycopyrrolate

Generic: glycopyrrolate
NDC Package

Package Facts

Identity

Package NDC 49884-065-01
Digits Only 4988406501
Product NDC 49884-065
Description

100 TABLET in 1 BOTTLE (49884-065-01)

Marketing

Marketing Status
Marketed Since 2006-09-26
Brand glycopyrrolate
Generic glycopyrrolate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b923cd6-6a35-4f2f-bcb8-cab438977a08", "openfda": {"upc": ["0349884066017", "0349884065010"], "unii": ["V92SO9WP2I"], "rxcui": ["197738", "197739"], "spl_set_id": ["1f266d77-4f9e-44c9-a000-2f8fea3ac80b"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (49884-065-01)", "package_ndc": "49884-065-01", "marketing_start_date": "20060926"}], "brand_name": "Glycopyrrolate", "product_id": "49884-065_1b923cd6-6a35-4f2f-bcb8-cab438977a08", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "49884-065", "generic_name": "glycopyrrolate", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glycopyrrolate", "active_ingredients": [{"name": "GLYCOPYRROLATE", "strength": "1 mg/1"}], "application_number": "ANDA040653", "marketing_category": "ANDA", "marketing_start_date": "20060926", "listing_expiration_date": "20261231"}