Package 69076-475-01

Brand: glycopyrrolate

Generic: glycopyrrolate
NDC Package

Package Facts

Identity

Package NDC 69076-475-01
Digits Only 6907647501
Product NDC 69076-475
Description

100 TABLET in 1 BOTTLE (69076-475-01)

Marketing

Marketing Status
Marketed Since 2021-05-01
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": "f03d88ab-275e-39b2-e053-2a95a90a22a6", "openfda": {"upc": ["0369076475014", "0369076476011"], "unii": ["V92SO9WP2I"], "rxcui": ["197738", "197739"], "spl_set_id": ["e1ded8e0-c05b-4bf4-a129-57d1726af6ed"], "manufacturer_name": ["Quinn Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69076-475-01)", "package_ndc": "69076-475-01", "marketing_start_date": "20210501"}], "brand_name": "GLYCOPYRROLATE", "product_id": "69076-475_f03d88ab-275e-39b2-e053-2a95a90a22a6", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "69076-475", "generic_name": "GLYCOPYRROLATE", "labeler_name": "Quinn Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GLYCOPYRROLATE", "active_ingredients": [{"name": "GLYCOPYRROLATE", "strength": "1 mg/1"}], "application_number": "ANDA091182", "marketing_category": "ANDA", "marketing_start_date": "20210501", "listing_expiration_date": "20261231"}