Package 0054-0045-44

Brand: ipratropium bromide

Generic: ipratropium bromide
NDC Package

Package Facts

Identity

Package NDC 0054-0045-44
Digits Only 0054004544
Product NDC 0054-0045
Product ID 0054-0045_c8dbb0db-5c00-4205-a765-d664117c4398
Description

1 BOTTLE, SPRAY in 1 CARTON (0054-0045-44) / 345 SPRAY in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2003-11-05
Brand ipratropium bromide
Generic ipratropium bromide
Sample Package No

Linked Drug Pages (1)

Ipratropium Bromide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "c8dbb0db-5c00-4205-a765-d664117c4398", "openfda": {"unii": ["J697UZ2A9J"], "rxcui": ["1797833"], "spl_set_id": ["05c56190-e346-4674-a4f8-049ce632ce2d"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (0054-0045-44)  / 345 SPRAY in 1 BOTTLE, SPRAY", "package_ndc": "0054-0045-44", "marketing_start_date": "20031105"}], "brand_name": "Ipratropium Bromide", "product_id": "0054-0045_c8dbb0db-5c00-4205-a765-d664117c4398", "dosage_form": "SPRAY", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "0054-0045", "generic_name": "Ipratropium Bromide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ipratropium Bromide", "active_ingredients": [{"name": "IPRATROPIUM BROMIDE", "strength": "21 ug/1"}], "application_number": "ANDA076664", "marketing_category": "ANDA", "marketing_start_date": "20031105", "listing_expiration_date": "20261231"}