Package 51467-005-01

Brand: coltalin

Generic: acetaminophen, chlorpheniramine maleate, phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51467-005-01
Digits Only 5146700501
Product NDC 51467-005
Product ID 51467-005_4abe57bb-45ad-ba3e-e063-6394a90a2df6
Description

2 BLISTER PACK in 1 BOX (51467-005-01) / 12 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2004-03-01
Brand coltalin
Generic acetaminophen, chlorpheniramine maleate, phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

COLTALIN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4abe57bb-45ad-ba3e-e063-6394a90a2df6", "openfda": {"unii": ["362O9ITL9D", "V1Q0O9OJ9Z", "04JA59TNSJ"], "rxcui": ["1046781"], "spl_set_id": ["01ab1152-06c9-4afe-8f2a-e110365275a5"], "manufacturer_name": ["FORTUNE PHARMACAL COMPANY LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 BOX (51467-005-01)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "51467-005-01", "marketing_start_date": "20040301"}, {"sample": false, "description": "3 BLISTER PACK in 1 BOX (51467-005-02)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "51467-005-02", "marketing_start_date": "20160426"}], "brand_name": "COLTALIN", "product_id": "51467-005_4abe57bb-45ad-ba3e-e063-6394a90a2df6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "51467-005", "generic_name": "Acetaminophen, Chlorpheniramine maleate, Phenylephrine hydrochloride", "labeler_name": "FORTUNE PHARMACAL COMPANY LIMITED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "COLTALIN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "CHLORPHENIRAMINE MALEATE", "strength": "2 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040301", "listing_expiration_date": "20271231"}