hydrocortisone butyrate
Generic: hydrocortisone butyrate
Labeler: taro pharmaceuticals u.s.a., inc.Drug Facts
Product Profile
Brand Name
hydrocortisone butyrate
Generic Name
hydrocortisone butyrate
Labeler
taro pharmaceuticals u.s.a., inc.
Dosage Form
OINTMENT
Routes
Active Ingredients
hydrocortisone butyrate 1 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
51672-4083
Product ID
51672-4083_26e4c766-6315-4c55-9814-181258a45ad5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076842
Listing Expiration
2026-12-31
Marketing Start
2004-12-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516724083
Hyphenated Format
51672-4083
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
ANDA076842 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/g
Packaging
- 1 TUBE in 1 CARTON (51672-4083-1) / 15 g in 1 TUBE
- 1 TUBE in 1 CARTON (51672-4083-2) / 30 g in 1 TUBE
- 5 g in 1 TUBE (51672-4083-5)
- 1 TUBE in 1 CARTON (51672-4083-6) / 45 g in 1 TUBE
- 1 TUBE in 1 CARTON (51672-4083-7) / 10 g in 1 TUBE
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "26e4c766-6315-4c55-9814-181258a45ad5", "openfda": {"unii": ["05RMF7YPWN"], "rxcui": ["1370758", "1370767", "1370770"], "spl_set_id": ["51176835-598d-4da7-8a00-6bd36f52aa82"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-4083-1) / 15 g in 1 TUBE", "package_ndc": "51672-4083-1", "marketing_start_date": "20041227"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-4083-2) / 30 g in 1 TUBE", "package_ndc": "51672-4083-2", "marketing_start_date": "20041227"}, {"sample": false, "description": "5 g in 1 TUBE (51672-4083-5)", "package_ndc": "51672-4083-5", "marketing_start_date": "20041227"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-4083-6) / 45 g in 1 TUBE", "package_ndc": "51672-4083-6", "marketing_start_date": "20041227"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-4083-7) / 10 g in 1 TUBE", "package_ndc": "51672-4083-7", "marketing_start_date": "20041227"}], "brand_name": "Hydrocortisone Butyrate", "product_id": "51672-4083_26e4c766-6315-4c55-9814-181258a45ad5", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-4083", "generic_name": "Hydrocortisone Butyrate", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocortisone Butyrate", "active_ingredients": [{"name": "HYDROCORTISONE BUTYRATE", "strength": "1 mg/g"}], "application_number": "ANDA076842", "marketing_category": "ANDA", "marketing_start_date": "20041227", "listing_expiration_date": "20261231"}