Package 84549-205-41

Brand: glycopyrrolate

Generic: glycopyrrolate
NDC Package

Package Facts

Identity

Package NDC 84549-205-41
Digits Only 8454920541
Product NDC 84549-205
Description

20 mL in 1 VIAL, GLASS (84549-205-41)

Marketing

Marketing Status
Marketed Since 2025-09-15
Brand glycopyrrolate
Generic glycopyrrolate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3edd6a26-dd0e-2411-e063-6394a90affa2", "openfda": {"unii": ["V92SO9WP2I"], "rxcui": ["238212"], "spl_set_id": ["3edd6a26-dd0f-2411-e063-6394a90affa2"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, GLASS (84549-205-41)", "package_ndc": "84549-205-41", "marketing_start_date": "20250915"}], "brand_name": "Glycopyrrolate", "product_id": "84549-205_3edd6a26-dd0e-2411-e063-6394a90affa2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "84549-205", "generic_name": "Glycopyrrolate", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glycopyrrolate", "active_ingredients": [{"name": "GLYCOPYRROLATE", "strength": ".2 mg/mL"}], "application_number": "ANDA210842", "marketing_category": "ANDA", "marketing_start_date": "20190711", "listing_expiration_date": "20261231"}