Package 71610-209-09

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-209-09
Digits Only 7161020909
Product NDC 71610-209
Description

9000 TABLET in 1 BOTTLE (71610-209-09)

Marketing

Marketing Status
Marketed Since 2018-12-18
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": "dcd1f50a-a200-48b3-89f7-039081a9e72d", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["da2c43f8-1c3a-447f-8994-f9899fb5e141"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "9000 TABLET in 1 BOTTLE (71610-209-09)", "package_ndc": "71610-209-09", "marketing_start_date": "20181218"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "71610-209_dcd1f50a-a200-48b3-89f7-039081a9e72d", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "71610-209", "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": "20 mg/1"}], "application_number": "ANDA040230", "marketing_category": "ANDA", "marketing_start_date": "19990226", "listing_expiration_date": "20261231"}