miconazole 7
Generic: miconazole nitrate
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
miconazole 7
Generic Name
miconazole nitrate
Labeler
preferred pharmaceuticals inc.
Dosage Form
CREAM
Routes
Active Ingredients
miconazole nitrate 20 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8661
Product ID
68788-8661_ee0e2b33-2eb1-482f-a324-2716c0f289fb
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA074164
Listing Expiration
2026-12-31
Marketing Start
2009-04-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888661
Hyphenated Format
68788-8661
Supplemental Identifiers
RxCUI
UNII
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
miconazole 7 (source: ndc)
Generic Name
miconazole nitrate (source: ndc)
Application Number
ANDA074164 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/g
Packaging
- 1 TUBE, WITH APPLICATOR in 1 CARTON (68788-8661-4) / 45 g in 1 TUBE, WITH APPLICATOR
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["VAGINAL"], "spl_id": "ee0e2b33-2eb1-482f-a324-2716c0f289fb", "openfda": {"unii": ["VW4H1CYW1K"], "rxcui": ["998540"], "spl_set_id": ["85a52081-d9cc-44f0-a8d3-851a45c4eb10"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 CARTON (68788-8661-4) / 45 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "68788-8661-4", "marketing_start_date": "20240513"}], "brand_name": "Miconazole 7", "product_id": "68788-8661_ee0e2b33-2eb1-482f-a324-2716c0f289fb", "dosage_form": "CREAM", "pharm_class": ["Azole Antifungal [EPC]", "Azoles [CS]"], "product_ndc": "68788-8661", "generic_name": "Miconazole Nitrate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Miconazole 7", "active_ingredients": [{"name": "MICONAZOLE NITRATE", "strength": "20 mg/g"}], "application_number": "ANDA074164", "marketing_category": "ANDA", "marketing_start_date": "20090421", "listing_expiration_date": "20261231"}