Package 70518-1767-2

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1767-2
Digits Only 7051817672
Product NDC 70518-1767
Product ID 70518-1767_497463c6-3cfc-e95c-e063-6294a90a4389
Description

20 TABLET in 1 BOTTLE, PLASTIC (70518-1767-2)

Marketing

Marketing Status
Marketed Since 2023-08-02
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": "497463c6-3cfc-e95c-e063-6294a90a4389", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["7ff96d1f-fb87-4244-a697-1d93e10eb738"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (70518-1767-2)", "package_ndc": "70518-1767-2", "marketing_start_date": "20230802"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "70518-1767_497463c6-3cfc-e95c-e063-6294a90a4389", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "70518-1767", "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": "ANDA040230", "marketing_category": "ANDA", "marketing_start_date": "20190102", "listing_expiration_date": "20271231"}