Package 0781-3825-96

Brand: glycopyrrolate

Generic: glycopyrrolate
NDC Package

Package Facts

Identity

Package NDC 0781-3825-96
Digits Only 0781382596
Product NDC 0781-3825
Description

25 VIAL in 1 CARTON (0781-3825-96) / 1 mL in 1 VIAL (0781-3825-71)

Marketing

Marketing Status
Marketed Since 2019-07-22
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": "eaf4151c-b7ea-4b3a-e053-2995a90adf17", "openfda": {"unii": ["V92SO9WP2I"], "rxcui": ["238212", "1731582", "1731590"], "spl_set_id": ["cb1ae370-ec4f-4114-9860-8f736f72b545"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0781-3825-96)  / 1 mL in 1 VIAL (0781-3825-71)", "package_ndc": "0781-3825-96", "marketing_start_date": "20190722"}], "brand_name": "Glycopyrrolate", "product_id": "0781-3825_eaf4151c-b7ea-4b3a-e053-2995a90adf17", "dosage_form": "INJECTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "0781-3825", "generic_name": "Glycopyrrolate", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glycopyrrolate", "active_ingredients": [{"name": "GLYCOPYRROLATE", "strength": ".2 mg/mL"}], "application_number": "ANDA211334", "marketing_category": "ANDA", "marketing_start_date": "20190722", "listing_expiration_date": "20261231"}