Package 16714-526-01

Brand: ipratropium bromide

Generic: ipratropium bromide
NDC Package

Package Facts

Identity

Package NDC 16714-526-01
Digits Only 1671452601
Product NDC 16714-526
Description

1 BOTTLE, SPRAY in 1 CARTON (16714-526-01) / 345 SPRAY, METERED in 1 BOTTLE, SPRAY

Marketing

Marketing Status
Marketed Since 2022-02-22
Brand ipratropium bromide
Generic ipratropium bromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "411659ee-987d-f755-47a7-eeba7c38a2c6", "openfda": {"unii": ["J697UZ2A9J"], "rxcui": ["1797833"], "spl_set_id": ["6493c00f-2306-2cb6-9624-4ea678f66576"], "manufacturer_name": ["NORTHSTAR RX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (16714-526-01)  / 345 SPRAY, METERED in 1 BOTTLE, SPRAY", "package_ndc": "16714-526-01", "marketing_start_date": "20220222"}], "brand_name": "Ipratropium Bromide", "product_id": "16714-526_411659ee-987d-f755-47a7-eeba7c38a2c6", "dosage_form": "SPRAY, METERED", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "16714-526", "generic_name": "Ipratropium Bromide", "labeler_name": "NORTHSTAR RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ipratropium Bromide", "active_ingredients": [{"name": "IPRATROPIUM BROMIDE", "strength": "21 ug/1"}], "application_number": "ANDA076156", "marketing_category": "ANDA", "marketing_start_date": "20220222", "listing_expiration_date": "20271231"}