ipratropium bromide
Generic: ipratropium bromide
Labeler: oceanside pharmaceuticalsDrug Facts
Product Profile
Brand Name
ipratropium bromide
Generic Name
ipratropium bromide
Labeler
oceanside pharmaceuticals
Dosage Form
SPRAY, METERED
Routes
Active Ingredients
ipratropium bromide 42 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
68682-399
Product ID
68682-399_bc46ff7c-14fd-4c47-a6e0-a87dda078099
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076103
Listing Expiration
2026-12-31
Marketing Start
2025-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68682399
Hyphenated Format
68682-399
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
ANDA076103 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 42 ug/1
Packaging
- 1 BOTTLE, SPRAY in 1 CARTON (68682-399-15) / 165 SPRAY, METERED 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": "bc46ff7c-14fd-4c47-a6e0-a87dda078099", "openfda": {"unii": ["J697UZ2A9J"], "rxcui": ["1797844"], "spl_set_id": ["b1a5e41a-9100-41d5-a7d0-2e763ad5efb6"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (68682-399-15) / 165 SPRAY, METERED in 1 BOTTLE, SPRAY", "package_ndc": "68682-399-15", "marketing_start_date": "20250601"}], "brand_name": "Ipratropium Bromide", "product_id": "68682-399_bc46ff7c-14fd-4c47-a6e0-a87dda078099", "dosage_form": "SPRAY, METERED", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "68682-399", "generic_name": "Ipratropium Bromide", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ipratropium Bromide", "active_ingredients": [{"name": "IPRATROPIUM BROMIDE", "strength": "42 ug/1"}], "application_number": "ANDA076103", "marketing_category": "ANDA", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}