mupirocin

Generic: mupirocin calcium

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

Drug Facts

Product Profile

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

mupirocin calcium 20 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-1370
Product ID 51672-1370_390bed79-7314-fbe9-e063-6394a90ae7f1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207116
Listing Expiration 2026-12-31
Marketing Start 2020-04-27

Pharmacologic Class

Classes
rna synthetase inhibitor antibacterial [epc] rna synthetase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516721370
Hyphenated Format 51672-1370

Supplemental Identifiers

RxCUI
311877
UNII
RG38I2P540

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 calcium (source: ndc)
Application Number ANDA207116 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51672-1370-1) / 15 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1370-2) / 30 g in 1 TUBE
source: ndc

Packages (2)

51672-1370-1 1 TUBE in 1 CARTON (51672-1370-1) / 15 g in 1 TUBE 51672-1370-2 1 TUBE in 1 CARTON (51672-1370-2) / 30 g in 1 TUBE

Ingredients (1)

mupirocin calcium (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": "390bed79-7314-fbe9-e063-6394a90ae7f1", "openfda": {"unii": ["RG38I2P540"], "rxcui": ["311877"], "spl_set_id": ["6719ffba-3430-4fa9-b65b-c5c195ee1b35"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1370-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1370-1", "marketing_start_date": "20200427"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1370-2)  / 30 g in 1 TUBE", "package_ndc": "51672-1370-2", "marketing_start_date": "20200427"}], "brand_name": "Mupirocin", "product_id": "51672-1370_390bed79-7314-fbe9-e063-6394a90ae7f1", "dosage_form": "CREAM", "pharm_class": ["RNA Synthetase Inhibitor Antibacterial [EPC]", "RNA Synthetase Inhibitors [MoA]"], "product_ndc": "51672-1370", "generic_name": "Mupirocin Calcium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mupirocin", "active_ingredients": [{"name": "MUPIROCIN CALCIUM", "strength": "20 mg/g"}], "application_number": "ANDA207116", "marketing_category": "ANDA", "marketing_start_date": "20200427", "listing_expiration_date": "20261231"}