Package 68071-3035-3

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3035-3
Digits Only 6807130353
Product NDC 68071-3035
Description

30 CAPSULE in 1 BOTTLE (68071-3035-3)

Marketing

Marketing Status
Marketed Since 2018-12-07
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": "1d8e280d-fb13-0e85-e063-6294a90a17a9", "openfda": {"upc": ["0368071303537"], "unii": ["CQ903KQA31"], "rxcui": ["991061"], "spl_set_id": ["7c75f650-c97d-06fa-e053-2991aa0a43bb"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-3035-3)", "package_ndc": "68071-3035-3", "marketing_start_date": "20181207"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "68071-3035_1d8e280d-fb13-0e85-e063-6294a90a17a9", "dosage_form": "CAPSULE", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "68071-3035", "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": "10 mg/1"}], "application_number": "ANDA084285", "marketing_category": "ANDA", "marketing_start_date": "19740930", "listing_expiration_date": "20261231"}