Package 68071-3555-6

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3555-6
Digits Only 6807135556
Product NDC 68071-3555
Description

60 TABLET in 1 BOTTLE (68071-3555-6)

Marketing

Marketing Status
Marketed Since 2023-12-21
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": "10abba06-dda8-24b2-e063-6394a90a7ae1", "openfda": {"upc": ["0368071355536"], "unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["0d07a460-5cb1-cd4b-e063-6294a90a291d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3555-3)", "package_ndc": "68071-3555-3", "marketing_start_date": "20231221"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3555-6)", "package_ndc": "68071-3555-6", "marketing_start_date": "20231221"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "68071-3555_10abba06-dda8-24b2-e063-6394a90a7ae1", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "68071-3555", "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": "ANDA040317", "marketing_category": "ANDA", "marketing_start_date": "20230425", "listing_expiration_date": "20261231"}