Package 68788-8581-3

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8581-3
Digits Only 6878885813
Product NDC 68788-8581
Product ID 68788-8581_48a98150-1118-4dab-8637-80ad223e24a2
Description

30 TABLET in 1 BOTTLE (68788-8581-3)

Marketing

Marketing Status
Marketed Since 2024-02-06
Brand dicyclomine hydrochloride
Generic dicyclomine hydrochloride
Sample Package No

Linked Drug Pages (1)

Dicyclomine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48a98150-1118-4dab-8637-80ad223e24a2", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["09f0bc6a-5aea-4618-8b71-22a2f0d036f8"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8581-3)", "package_ndc": "68788-8581-3", "marketing_start_date": "20240206"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "68788-8581_48a98150-1118-4dab-8637-80ad223e24a2", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "68788-8581", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA040317", "marketing_category": "ANDA", "marketing_start_date": "20240206", "listing_expiration_date": "20261231"}