mupirocin

Generic: mupirocin

Labeler: atlantic biologicals corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mupirocin
Generic Name mupirocin
Labeler atlantic biologicals corp.
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

mupirocin 20 mg/g

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-0112
Product ID 17856-0112_3633ac1b-d811-2f7b-e063-6394a90a1227
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065123
Listing Expiration 2026-12-31
Marketing Start 2009-10-30

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 178560112
Hyphenated Format 17856-0112

Supplemental Identifiers

RxCUI
106346
UNII
D0GX863OA5
NUI
N0000175515 N0000175516

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 ANDA065123 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/g
source: ndc
Packaging
  • 1 g in 1 SYRINGE (17856-0112-1)
source: ndc

Packages (1)

Ingredients (1)

mupirocin (20 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3633ac1b-d811-2f7b-e063-6394a90a1227", "openfda": {"nui": ["N0000175515", "N0000175516"], "unii": ["D0GX863OA5"], "rxcui": ["106346"], "spl_set_id": ["da2f7d4e-82c6-4790-8eea-3a97e5b30734"], "pharm_class_epc": ["RNA Synthetase Inhibitor Antibacterial [EPC]"], "pharm_class_moa": ["RNA Synthetase Inhibitors [MoA]"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "1 g in 1 SYRINGE (17856-0112-1)", "package_ndc": "17856-0112-1", "marketing_start_date": "20240508"}], "brand_name": "mupirocin", "product_id": "17856-0112_3633ac1b-d811-2f7b-e063-6394a90a1227", "dosage_form": "OINTMENT", "pharm_class": ["RNA Synthetase Inhibitor Antibacterial [EPC]", "RNA Synthetase Inhibitors [MoA]"], "product_ndc": "17856-0112", "generic_name": "Mupirocin", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "mupirocin", "active_ingredients": [{"name": "MUPIROCIN", "strength": "20 mg/g"}], "application_number": "ANDA065123", "marketing_category": "ANDA", "marketing_start_date": "20091030", "listing_expiration_date": "20261231"}