Package 68071-3916-6

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3916-6
Digits Only 6807139166
Product NDC 68071-3916
Description

6 TABLET in 1 BOTTLE (68071-3916-6)

Marketing

Marketing Status
Marketed Since 2025-11-18
Brand dicyclomine hydrochloride
Generic dicyclomine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43e30b73-4779-d722-e063-6394a90a51de", "openfda": {"upc": ["0368071391664"], "unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["43e30378-6376-caab-e063-6294a90a8696"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (68071-3916-6)", "package_ndc": "68071-3916-6", "marketing_start_date": "20251118"}], "brand_name": "Dicyclomine hydrochloride", "product_id": "68071-3916_43e30b73-4779-d722-e063-6394a90a51de", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "68071-3916", "generic_name": "Dicyclomine hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA217566", "marketing_category": "ANDA", "marketing_start_date": "20240507", "listing_expiration_date": "20261231"}