Package 68071-3645-3

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3645-3
Digits Only 6807136453
Product NDC 68071-3645
Product ID 68071-3645_2a2fc3d8-0b13-ac40-e063-6394a90a5a3d
Description

30 TABLET in 1 BOTTLE, PLASTIC (68071-3645-3)

Marketing

Marketing Status
Marketed Since 2024-07-10
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": "2a2fc3d8-0b13-ac40-e063-6394a90a5a3d", "openfda": {"upc": ["0368071364538"], "unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["1cebadd3-2c45-9cff-e063-6394a90aaceb"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68071-3645-3)", "package_ndc": "68071-3645-3", "marketing_start_date": "20240710"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "68071-3645_2a2fc3d8-0b13-ac40-e063-6394a90a5a3d", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "68071-3645", "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": "ANDA216782", "marketing_category": "ANDA", "marketing_start_date": "20230701", "listing_expiration_date": "20261231"}