mupirocin
Generic: mupirocin
Labeler: atlantic biologicals corp.Drug Facts
Product Profile
Brand Name
mupirocin
Generic Name
mupirocin
Labeler
atlantic biologicals corp.
Dosage Form
OINTMENT
Routes
Active Ingredients
mupirocin 20 mg/g
Manufacturer
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)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
178560112
Hyphenated Format
17856-0112
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 20 mg/g
Packaging
- 1 g in 1 SYRINGE (17856-0112-1)
Packages (1)
Ingredients (1)
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"}