Package 70518-4432-0

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4432-0
Digits Only 7051844320
Product NDC 70518-4432
Description

30 CAPSULE in 1 BLISTER PACK (70518-4432-0)

Marketing

Marketing Status
Marketed Since 2025-08-12
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": "3c2eea67-bae1-297c-e063-6394a90a13f2", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991061"], "spl_set_id": ["8652905b-b3f1-4eed-bde8-ce507186ae9a"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4432-0)", "package_ndc": "70518-4432-0", "marketing_start_date": "20250812"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "70518-4432_3c2eea67-bae1-297c-e063-6394a90a13f2", "dosage_form": "CAPSULE", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "70518-4432", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA217054", "marketing_category": "ANDA", "marketing_start_date": "20250812", "listing_expiration_date": "20261231"}