Package 60760-802-30

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-802-30
Digits Only 6076080230
Product NDC 60760-802
Product ID 60760-802_41aecc7f-7307-438a-e063-6294a90a85bb
Description

30 TABLET in 1 BOTTLE, PLASTIC (60760-802-30)

Marketing

Marketing Status
Marketed Since 2025-10-21
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": "41aecc7f-7307-438a-e063-6294a90a85bb", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["41aed1c9-b32f-3694-e063-6394a90a29e4"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-802-30)", "package_ndc": "60760-802-30", "marketing_start_date": "20251021"}], "brand_name": "Dicyclomine hydrochloride", "product_id": "60760-802_41aecc7f-7307-438a-e063-6294a90a85bb", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "60760-802", "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": "ANDA216736", "marketing_category": "ANDA", "marketing_start_date": "20221214", "listing_expiration_date": "20261231"}