mupirocin

Generic: mupirocin

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mupirocin
Generic Name mupirocin
Labeler sun pharmaceutical industries, inc.
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

mupirocin 20 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-1312
Product ID 51672-1312_3961a44e-34c2-d648-e063-6394a90a974e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065170
Listing Expiration 2026-12-31
Marketing Start 2005-09-23

Pharmacologic Class

Established (EPC)
rna synthetase inhibitor antibacterial [epc]
Mechanism of Action
rna synthetase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516721312
Hyphenated Format 51672-1312

Supplemental Identifiers

RxCUI
106346
UNII
D0GX863OA5
NUI
N0000175515 N0000175516

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name mupirocin (source: ndc)
Generic Name mupirocin (source: ndc)
Application Number ANDA065170 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51672-1312-0) / 22 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1312-1) / 15 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1312-2) / 30 g in 1 TUBE
source: ndc

Packages (3)

51672-1312-0 1 TUBE in 1 CARTON (51672-1312-0) / 22 g in 1 TUBE 51672-1312-1 1 TUBE in 1 CARTON (51672-1312-1) / 15 g in 1 TUBE 51672-1312-2 1 TUBE in 1 CARTON (51672-1312-2) / 30 g in 1 TUBE

Ingredients (1)

mupirocin (20 mg/g)

Linked Drug Pages (1)

Mupirocin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3961a44e-34c2-d648-e063-6394a90a974e", "openfda": {"nui": ["N0000175515", "N0000175516"], "unii": ["D0GX863OA5"], "rxcui": ["106346"], "spl_set_id": ["900bb675-2f03-47e3-854e-257ec4831332"], "pharm_class_epc": ["RNA Synthetase Inhibitor Antibacterial [EPC]"], "pharm_class_moa": ["RNA Synthetase Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1312-0)  / 22 g in 1 TUBE", "package_ndc": "51672-1312-0", "marketing_start_date": "20050923"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1312-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1312-1", "marketing_start_date": "20050923"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1312-2)  / 30 g in 1 TUBE", "package_ndc": "51672-1312-2", "marketing_start_date": "20050923"}], "brand_name": "Mupirocin", "product_id": "51672-1312_3961a44e-34c2-d648-e063-6394a90a974e", "dosage_form": "OINTMENT", "pharm_class": ["RNA Synthetase Inhibitor Antibacterial [EPC]", "RNA Synthetase Inhibitors [MoA]"], "product_ndc": "51672-1312", "generic_name": "Mupirocin", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mupirocin", "active_ingredients": [{"name": "MUPIROCIN", "strength": "20 mg/g"}], "application_number": "ANDA065170", "marketing_category": "ANDA", "marketing_start_date": "20050923", "listing_expiration_date": "20261231"}