hydrocortisone valerate

Generic: hydrocortisone valerate

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

Drug Facts

Product Profile

Brand Name hydrocortisone valerate
Generic Name hydrocortisone valerate
Labeler sun pharmaceutical industries, inc.
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

hydrocortisone valerate 2 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-1292
Product ID 51672-1292_39628349-b388-4030-e063-6394a90a6ce9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075043
Listing Expiration 2026-12-31
Marketing Start 1998-08-25

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516721292
Hyphenated Format 51672-1292

Supplemental Identifiers

RxCUI
1370750 1370754
UNII
68717P8FUZ

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 hydrocortisone valerate (source: ndc)
Generic Name hydrocortisone valerate (source: ndc)
Application Number ANDA075043 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51672-1292-1) / 15 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1292-3) / 60 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1292-6) / 45 g in 1 TUBE
source: ndc

Packages (3)

51672-1292-1 1 TUBE in 1 CARTON (51672-1292-1) / 15 g in 1 TUBE 51672-1292-3 1 TUBE in 1 CARTON (51672-1292-3) / 60 g in 1 TUBE 51672-1292-6 1 TUBE in 1 CARTON (51672-1292-6) / 45 g in 1 TUBE

Ingredients (1)

hydrocortisone valerate (2 mg/g)

Linked Drug Pages (1)

Hydrocortisone Valerate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "39628349-b388-4030-e063-6394a90a6ce9", "openfda": {"unii": ["68717P8FUZ"], "rxcui": ["1370750", "1370754"], "spl_set_id": ["a9011d6f-6808-48a7-ab6b-df8d40540570"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1292-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1292-1", "marketing_start_date": "19980825"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1292-3)  / 60 g in 1 TUBE", "package_ndc": "51672-1292-3", "marketing_start_date": "19980825"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1292-6)  / 45 g in 1 TUBE", "package_ndc": "51672-1292-6", "marketing_start_date": "19980825"}], "brand_name": "Hydrocortisone Valerate", "product_id": "51672-1292_39628349-b388-4030-e063-6394a90a6ce9", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1292", "generic_name": "Hydrocortisone Valerate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocortisone Valerate", "active_ingredients": [{"name": "HYDROCORTISONE VALERATE", "strength": "2 mg/g"}], "application_number": "ANDA075043", "marketing_category": "ANDA", "marketing_start_date": "19980825", "listing_expiration_date": "20261231"}