Package 70518-4555-0

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4555-0
Digits Only 7051845550
Product NDC 70518-4555
Product ID 70518-4555_495f07c3-dbed-f7be-e063-6294a90a9d61
Description

180 TABLET in 1 BOTTLE, PLASTIC (70518-4555-0)

Marketing

Marketing Status
Marketed Since 2026-01-26
Brand dicyclomine hydrochloride
Generic dicyclomine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "495f07c3-dbed-f7be-e063-6294a90a9d61", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["380270a8-d0a6-44cb-bb34-f91db6e6ac71"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-4555-0)", "package_ndc": "70518-4555-0", "marketing_start_date": "20260126"}], "brand_name": "Dicyclomine hydrochloride", "product_id": "70518-4555_495f07c3-dbed-f7be-e063-6294a90a9d61", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "70518-4555", "generic_name": "Dicyclomine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA217566", "marketing_category": "ANDA", "marketing_start_date": "20260126", "listing_expiration_date": "20271231"}