Package 69452-311-32

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69452-311-32
Digits Only 6945231132
Product NDC 69452-311
Description

1000 TABLET in 1 BOTTLE, PLASTIC (69452-311-32)

Marketing

Marketing Status
Marketed Since 2024-05-23
Brand dicyclomine hydrochloride
Generic dicyclomine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1927b1f0-6fee-f127-e063-6394a90a05a3", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["051bfee3-06cf-309a-e063-6394a90a0bb3"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (69452-311-20)", "package_ndc": "69452-311-20", "marketing_start_date": "20230913"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (69452-311-32)", "package_ndc": "69452-311-32", "marketing_start_date": "20240523"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "69452-311_1927b1f0-6fee-f127-e063-6394a90a05a3", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "69452-311", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA217916", "marketing_category": "ANDA", "marketing_start_date": "20230913", "listing_expiration_date": "20261231"}