hydrocortisone butyrate
Generic: hydrocortisone butyrate
Labeler: oceanside pharmaceuticalsDrug Facts
Product Profile
Brand Name
hydrocortisone butyrate
Generic Name
hydrocortisone butyrate
Labeler
oceanside pharmaceuticals
Dosage Form
OINTMENT
Routes
Active Ingredients
hydrocortisone butyrate 1 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
68682-271
Product ID
68682-271_01f93fa6-5fea-4b3e-aa41-e8e0269257ee
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018652
Listing Expiration
2026-12-31
Marketing Start
2009-09-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68682271
Hyphenated Format
68682-271
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
hydrocortisone butyrate (source: ndc)
Generic Name
hydrocortisone butyrate (source: ndc)
Application Number
NDA018652 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/g
Packaging
- 1 TUBE in 1 CARTON (68682-271-15) / 15 g in 1 TUBE
- 1 TUBE in 1 CARTON (68682-271-45) / 45 g in 1 TUBE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "01f93fa6-5fea-4b3e-aa41-e8e0269257ee", "openfda": {"unii": ["05RMF7YPWN"], "rxcui": ["1370758"], "spl_set_id": ["7c3f8417-7861-41e3-876f-9b82aff7d1a0"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68682-271-15) / 15 g in 1 TUBE", "package_ndc": "68682-271-15", "marketing_start_date": "20090901"}, {"sample": false, "description": "1 TUBE in 1 CARTON (68682-271-45) / 45 g in 1 TUBE", "package_ndc": "68682-271-45", "marketing_start_date": "20090901"}], "brand_name": "Hydrocortisone Butyrate", "product_id": "68682-271_01f93fa6-5fea-4b3e-aa41-e8e0269257ee", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68682-271", "generic_name": "hydrocortisone butyrate", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocortisone Butyrate", "active_ingredients": [{"name": "HYDROCORTISONE BUTYRATE", "strength": "1 mg/g"}], "application_number": "NDA018652", "marketing_category": "NDA", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}