miconazorb af

Generic: miconazole nitrate

Labeler: amerisourcebergen drug corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name miconazorb af
Generic Name miconazole nitrate
Labeler amerisourcebergen drug corporation
Dosage Form POWDER
Routes
TOPICAL
Active Ingredients

miconazole nitrate 20 mg/g

Manufacturer
AmerisourceBergen Drug Corporation

Identifiers & Regulatory

Product NDC 46122-789
Product ID 46122-789_42642785-742d-6084-e063-6294a90abf74
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M005
Listing Expiration 2026-12-31
Marketing Start 2024-04-05

Pharmacologic Class

Classes
azole antifungal [epc] azoles [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 46122789
Hyphenated Format 46122-789

Supplemental Identifiers

RxCUI
998461
UPC
0346122789295
UNII
VW4H1CYW1K

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 miconazorb af (source: ndc)
Generic Name miconazole nitrate (source: ndc)
Application Number M005 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/g
source: ndc
Packaging
  • 71 g in 1 BOTTLE, PLASTIC (46122-789-29)
source: ndc

Packages (1)

Ingredients (1)

miconazole nitrate (20 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "42642785-742d-6084-e063-6294a90abf74", "openfda": {"upc": ["0346122789295"], "unii": ["VW4H1CYW1K"], "rxcui": ["998461"], "spl_set_id": ["13a20d21-42d5-fe56-e063-6394a90aaf57"], "manufacturer_name": ["AmerisourceBergen Drug Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "71 g in 1 BOTTLE, PLASTIC (46122-789-29)", "package_ndc": "46122-789-29", "marketing_start_date": "20240405"}], "brand_name": "Miconazorb AF", "product_id": "46122-789_42642785-742d-6084-e063-6294a90abf74", "dosage_form": "POWDER", "pharm_class": ["Azole Antifungal [EPC]", "Azoles [CS]"], "product_ndc": "46122-789", "generic_name": "Miconazole Nitrate", "labeler_name": "AmerisourceBergen Drug Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Miconazorb AF", "active_ingredients": [{"name": "MICONAZOLE NITRATE", "strength": "20 mg/g"}], "application_number": "M005", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240405", "listing_expiration_date": "20261231"}