betamethasone valerate

Generic: betamethasone valerate

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

Drug Facts

Product Profile

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

betamethasone valerate 1 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-1269
Product ID 51672-1269_40339862-869b-f954-e063-6294a90a9add
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072041
Listing Expiration 2026-12-31
Marketing Start 1988-01-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516721269
Hyphenated Format 51672-1269

Supplemental Identifiers

RxCUI
197407
UPC
0351672126919
UNII
9IFA5XM7R2

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 betamethasone valerate (source: ndc)
Generic Name betamethasone valerate (source: ndc)
Application Number ANDA072041 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51672-1269-1) / 15 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1269-6) / 45 g in 1 TUBE
source: ndc

Packages (2)

51672-1269-1 1 TUBE in 1 CARTON (51672-1269-1) / 15 g in 1 TUBE 51672-1269-6 1 TUBE in 1 CARTON (51672-1269-6) / 45 g in 1 TUBE

Ingredients (1)

betamethasone valerate (1 mg/g)

Linked Drug Pages (1)

BETAMETHASONE VALERATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "40339862-869b-f954-e063-6294a90a9add", "openfda": {"upc": ["0351672126919"], "unii": ["9IFA5XM7R2"], "rxcui": ["197407"], "spl_set_id": ["3c85be0f-2731-44f1-a18e-d3852d54846f"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1269-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1269-1", "marketing_start_date": "19880106"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1269-6)  / 45 g in 1 TUBE", "package_ndc": "51672-1269-6", "marketing_start_date": "19880106"}], "brand_name": "BETAMETHASONE VALERATE", "product_id": "51672-1269_40339862-869b-f954-e063-6294a90a9add", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1269", "generic_name": "Betamethasone Valerate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BETAMETHASONE VALERATE", "active_ingredients": [{"name": "BETAMETHASONE VALERATE", "strength": "1 mg/g"}], "application_number": "ANDA072041", "marketing_category": "ANDA", "marketing_start_date": "19880106", "listing_expiration_date": "20261231"}