Package 0615-8483-39

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8483-39
Digits Only 0615848339
Product NDC 0615-8483
Description

30 CAPSULE in 1 BLISTER PACK (0615-8483-39)

Marketing

Marketing Status
Marketed Since 2023-08-15
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": "d6f45cf6-4b7c-4248-9cea-614df0a3dc96", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991061"], "spl_set_id": ["a16e7b6b-dbc9-463d-9bde-dba4f25589cf"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (0615-8483-39)", "package_ndc": "0615-8483-39", "marketing_start_date": "20230815"}], "brand_name": "Dicyclomine hydrochloride", "product_id": "0615-8483_d6f45cf6-4b7c-4248-9cea-614df0a3dc96", "dosage_form": "CAPSULE", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "0615-8483", "generic_name": "Dicyclomine hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040204", "marketing_category": "ANDA", "marketing_start_date": "19970228", "listing_expiration_date": "20261231"}