Package 71610-265-09

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-265-09
Digits Only 7161026509
Product NDC 71610-265
Description

9000 CAPSULE in 1 BOTTLE (71610-265-09)

Marketing

Marketing Status
Marketed Since 2019-04-25
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": "c5c78781-b840-4c6b-ad40-968ab2ae25ad", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991061"], "spl_set_id": ["860e8ea6-6f9b-4fe6-a23d-3600b69c0b35"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "9000 CAPSULE in 1 BOTTLE (71610-265-09)", "package_ndc": "71610-265-09", "marketing_start_date": "20190425"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "71610-265_c5c78781-b840-4c6b-ad40-968ab2ae25ad", "dosage_form": "CAPSULE", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "71610-265", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA084285", "marketing_category": "ANDA", "marketing_start_date": "19740930", "listing_expiration_date": "20261231"}