Package 68682-398-30

Brand: ipratroprium bromide

Generic: ipratroprium bromide
NDC Package

Package Facts

Identity

Package NDC 68682-398-30
Digits Only 6868239830
Product NDC 68682-398
Description

1 BOTTLE, SPRAY in 1 CARTON (68682-398-30) / 345 SPRAY, METERED in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2025-06-01
Brand ipratroprium bromide
Generic ipratroprium bromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "b9d78453-9a78-4777-908f-a46a34f09cb1", "openfda": {"unii": ["J697UZ2A9J"], "rxcui": ["1797833"], "spl_set_id": ["40e37c2f-a2c0-419b-8451-1aa0458bc420"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (68682-398-30)  / 345 SPRAY, METERED in 1 BOTTLE, SPRAY", "package_ndc": "68682-398-30", "marketing_start_date": "20250601"}], "brand_name": "Ipratroprium Bromide", "product_id": "68682-398_b9d78453-9a78-4777-908f-a46a34f09cb1", "dosage_form": "SPRAY, METERED", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "68682-398", "generic_name": "Ipratroprium Bromide", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ipratroprium Bromide", "active_ingredients": [{"name": "IPRATROPIUM BROMIDE", "strength": "21 ug/1"}], "application_number": "ANDA076025", "marketing_category": "ANDA", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}