Package 49884-042-33

Brand: glycopyrrolate

Generic: glycopyrrolate
NDC Package

Package Facts

Identity

Package NDC 49884-042-33
Digits Only 4988404233
Product NDC 49884-042
Description

16 mL in 1 BOTTLE (49884-042-33)

Marketing

Marketing Status
Marketed Since 2022-01-04
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": "afe8b809-9378-4d06-8965-5e30b2deb18d", "openfda": {"unii": ["V92SO9WP2I"], "rxcui": ["999961"], "spl_set_id": ["ff65c5d3-7ba9-4315-a884-199151eb45a5"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "16 mL in 1 BOTTLE (49884-042-33)", "package_ndc": "49884-042-33", "marketing_start_date": "20220104"}], "brand_name": "Glycopyrrolate", "product_id": "49884-042_afe8b809-9378-4d06-8965-5e30b2deb18d", "dosage_form": "SOLUTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "49884-042", "generic_name": "Glycopyrrolate", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glycopyrrolate", "active_ingredients": [{"name": "GLYCOPYRROLATE", "strength": "1 mg/5mL"}], "application_number": "ANDA204438", "marketing_category": "ANDA", "marketing_start_date": "20220104", "listing_expiration_date": "20261231"}