oxiconazole nitrate

Generic: oxiconazole nitrate

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

Drug Facts

Product Profile

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

oxiconazole nitrate 10 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-1359
Product ID 51672-1359_38efa4f4-a3f2-fd03-e063-6394a90aac00
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205076
Listing Expiration 2026-12-31
Marketing Start 2016-03-07

Pharmacologic Class

Classes
azole antifungal [epc] azoles [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516721359
Hyphenated Format 51672-1359

Supplemental Identifiers

RxCUI
312139
UNII
RQ8UL4C17S

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 oxiconazole nitrate (source: ndc)
Generic Name oxiconazole nitrate (source: ndc)
Application Number ANDA205076 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51672-1359-1) / 15 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1359-2) / 30 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1359-3) / 60 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1359-8) / 90 g in 1 TUBE
source: ndc

Packages (4)

Ingredients (1)

oxiconazole nitrate (10 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "38efa4f4-a3f2-fd03-e063-6394a90aac00", "openfda": {"unii": ["RQ8UL4C17S"], "rxcui": ["312139"], "spl_set_id": ["04477378-cccc-4db3-9e1b-5c1d6a00bd13"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1359-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1359-1", "marketing_start_date": "20160307"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1359-2)  / 30 g in 1 TUBE", "package_ndc": "51672-1359-2", "marketing_start_date": "20160307"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1359-3)  / 60 g in 1 TUBE", "package_ndc": "51672-1359-3", "marketing_start_date": "20160307"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1359-8)  / 90 g in 1 TUBE", "package_ndc": "51672-1359-8", "marketing_start_date": "20160307"}], "brand_name": "Oxiconazole Nitrate", "product_id": "51672-1359_38efa4f4-a3f2-fd03-e063-6394a90aac00", "dosage_form": "CREAM", "pharm_class": ["Azole Antifungal [EPC]", "Azoles [CS]"], "product_ndc": "51672-1359", "generic_name": "Oxiconazole Nitrate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxiconazole Nitrate", "active_ingredients": [{"name": "OXICONAZOLE NITRATE", "strength": "10 mg/g"}], "application_number": "ANDA205076", "marketing_category": "ANDA", "marketing_start_date": "20160307", "listing_expiration_date": "20261231"}