ipratropium bromide
Generic: ipratropium bromide
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
ipratropium bromide
Generic Name
ipratropium bromide
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
SPRAY
Routes
Active Ingredients
ipratropium bromide 21 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
0054-0045
Product ID
0054-0045_c8dbb0db-5c00-4205-a765-d664117c4398
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076664
Listing Expiration
2026-12-31
Marketing Start
2003-11-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00540045
Hyphenated Format
0054-0045
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ipratropium bromide (source: ndc)
Generic Name
ipratropium bromide (source: ndc)
Application Number
ANDA076664 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 21 ug/1
Packaging
- 1 BOTTLE, SPRAY in 1 CARTON (0054-0045-44) / 345 SPRAY in 1 BOTTLE, SPRAY
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}