Package 0054-0046-41

Brand: ipratropium bromide

Generic: ipratropium bromide
NDC Package

Package Facts

Identity

Package NDC 0054-0046-41
Digits Only 0054004641
Product NDC 0054-0046
Product ID 0054-0046_1af1d74f-a67d-450a-ab96-1021079f5a35
Description

1 BOTTLE, SPRAY in 1 CARTON (0054-0046-41) / 165 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": "1af1d74f-a67d-450a-ab96-1021079f5a35", "openfda": {"unii": ["J697UZ2A9J"], "rxcui": ["1797844"], "spl_set_id": ["71bdbbb9-8696-416d-bed4-7259929c0161"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (0054-0046-41)  / 165 SPRAY in 1 BOTTLE, SPRAY", "package_ndc": "0054-0046-41", "marketing_start_date": "20031105"}], "brand_name": "Ipratropium Bromide", "product_id": "0054-0046_1af1d74f-a67d-450a-ab96-1021079f5a35", "dosage_form": "SPRAY", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "0054-0046", "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": "42 ug/1"}], "application_number": "ANDA076598", "marketing_category": "ANDA", "marketing_start_date": "20031105", "listing_expiration_date": "20261231"}