Package 42708-160-56

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-160-56
Digits Only 4270816056
Product NDC 42708-160
Description

56 CAPSULE in 1 BOTTLE, PLASTIC (42708-160-56)

Marketing

Marketing Status
Marketed Since 2023-03-01
Brand dicyclomine hydrochloride
Generic dicyclomine hydrochloride
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459bd8c8-e637-3bce-e063-6294a90af1ed", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991061"], "spl_set_id": ["f5dd6ecc-440d-6c47-e053-2a95a90a92d3"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "56 CAPSULE in 1 BOTTLE, PLASTIC (42708-160-56)", "package_ndc": "42708-160-56", "marketing_start_date": "20230301"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "42708-160_459bd8c8-e637-3bce-e063-6294a90af1ed", "dosage_form": "CAPSULE", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "42708-160", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA085082", "marketing_category": "ANDA", "marketing_start_date": "19860619", "listing_expiration_date": "20261231"}