Package 0615-8561-39

Brand: dicyclomine

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8561-39
Digits Only 0615856139
Product NDC 0615-8561
Description

30 TABLET in 1 BLISTER PACK (0615-8561-39)

Marketing

Marketing Status
Discontinued 2026-05-31
Brand dicyclomine
Generic dicyclomine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c441cf93-8640-4a93-9be2-86c751358a31", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["a48a5b44-3812-4544-82d8-660763d76fd3"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8561-39)", "package_ndc": "0615-8561-39", "marketing_end_date": "20260531", "marketing_start_date": "20250213"}], "brand_name": "Dicyclomine", "product_id": "0615-8561_c441cf93-8640-4a93-9be2-86c751358a31", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "0615-8561", "generic_name": "Dicyclomine hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA040161", "marketing_category": "ANDA", "marketing_end_date": "20260531", "marketing_start_date": "19961001"}