Package 70518-4393-0

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4393-0
Digits Only 7051843930
Product NDC 70518-4393
Product ID 70518-4393_3a0ce845-ca16-a1f1-e063-6294a90ab259
Description

30 TABLET in 1 BLISTER PACK (70518-4393-0)

Marketing

Marketing Status
Marketed Since 2025-07-16
Brand dicyclomine hydrochloride
Generic dicyclomine hydrochloride
Sample Package No

Linked Drug Pages (1)

Dicyclomine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a0ce845-ca16-a1f1-e063-6294a90ab259", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["62be6437-db8c-431b-8e5f-780487cf2d43"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4393-0)", "package_ndc": "70518-4393-0", "marketing_start_date": "20250716"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "70518-4393_3a0ce845-ca16-a1f1-e063-6294a90ab259", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "70518-4393", "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": "ANDA040317", "marketing_category": "ANDA", "marketing_start_date": "20250716", "listing_expiration_date": "20261231"}