Package 51672-2027-1

Brand: triple antibiotic plus pain relief

Generic: bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51672-2027-1
Digits Only 5167220271
Product NDC 51672-2027
Description

1 TUBE in 1 CARTON (51672-2027-1) / 14.2 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2012-03-31
Brand triple antibiotic plus pain relief
Generic bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "38e4b68f-68c3-c5df-e063-6294a90a033a", "openfda": {"unii": ["89Y4M234ES", "057Y626693", "19371312D4", "88AYB867L5"], "rxcui": ["1359350"], "spl_set_id": ["4545c043-8e8e-4288-b4d8-e6ec9d72f979"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-2027-1)  / 14.2 g in 1 TUBE", "package_ndc": "51672-2027-1", "marketing_start_date": "20120331"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-2027-2)  / 28.4 g in 1 TUBE", "package_ndc": "51672-2027-2", "marketing_start_date": "20120331"}], "brand_name": "Triple Antibiotic Plus Pain Relief", "product_id": "51672-2027_38e4b68f-68c3-c5df-e063-6294a90a033a", "dosage_form": "OINTMENT", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]", "Decreased Cell Wall Synthesis & Repair [PE]", "Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "51672-2027", "generic_name": "Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Triple Antibiotic Plus Pain Relief", "active_ingredients": [{"name": "BACITRACIN ZINC", "strength": "500 [USP'U]/g"}, {"name": "NEOMYCIN SULFATE", "strength": "3.5 mg/g"}, {"name": "POLYMYXIN B SULFATE", "strength": "10000 [USP'U]/g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120331", "listing_expiration_date": "20261231"}