Package 0781-3831-95
Brand: glycopyrrolate
Generic: glycopyrrolatePackage Facts
Identity
Package NDC
0781-3831-95
Digits Only
0781383195
Product NDC
0781-3831
Description
10 VIAL in 1 CARTON (0781-3831-95) / 20 mL in 1 VIAL (0781-3831-80)
Marketing
Marketing Status
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": "10 VIAL in 1 CARTON (0781-3831-95) / 20 mL in 1 VIAL (0781-3831-80)", "package_ndc": "0781-3831-95", "marketing_start_date": "20190722"}], "brand_name": "Glycopyrrolate", "product_id": "0781-3831_eaf4151c-b7ea-4b3a-e053-2995a90adf17", "dosage_form": "INJECTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "0781-3831", "generic_name": "Glycopyrrolate", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glycopyrrolate", "active_ingredients": [{"name": "GLYCOPYRROLATE", "strength": "4 mg/20mL"}], "application_number": "ANDA211334", "marketing_category": "ANDA", "marketing_start_date": "20190722", "listing_expiration_date": "20261231"}