Package 60760-931-30

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-931-30
Digits Only 6076093130
Product NDC 60760-931
Product ID 60760-931_2ad03e27-9bb0-18ab-e063-6394a90af4fc
Description

30 TABLET in 1 BOTTLE, PLASTIC (60760-931-30)

Marketing

Marketing Status
Marketed Since 2024-12-30
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": "2ad03e27-9bb0-18ab-e063-6394a90af4fc", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["2ad04535-1c34-6c5c-e063-6294a90a0c17"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-931-30)", "package_ndc": "60760-931-30", "marketing_start_date": "20241230"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "60760-931_2ad03e27-9bb0-18ab-e063-6394a90af4fc", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "60760-931", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA216782", "marketing_category": "ANDA", "marketing_start_date": "20230701", "listing_expiration_date": "20261231"}