betamethasone valerate

Generic: betamethasone valerate

Labeler: e. fougera & co. a division of fougera pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name betamethasone valerate
Generic Name betamethasone valerate
Labeler e. fougera & co. a division of fougera pharmaceuticals, llc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

betamethasone valerate 1 mg/g

Manufacturer
E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 0168-0040
Product ID 0168-0040_41e96a74-4120-436e-97e5-2dc62af84b2a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018861
Listing Expiration 2027-12-31
Marketing Start 1983-08-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01680040
Hyphenated Format 0168-0040

Supplemental Identifiers

RxCUI
197407 197408 197409
UPC
0301680040158
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 NDA018861 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/g
source: ndc
Packaging
  • 15 g in 1 TUBE (0168-0040-15)
  • 45 g in 1 TUBE (0168-0040-46)
source: ndc

Packages (2)

Ingredients (1)

betamethasone valerate (1 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "41e96a74-4120-436e-97e5-2dc62af84b2a", "openfda": {"upc": ["0301680040158"], "unii": ["9IFA5XM7R2"], "rxcui": ["197407", "197408", "197409"], "spl_set_id": ["0b386ccc-a2d4-4d18-a2d7-e46ff894c674"], "manufacturer_name": ["E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 g in 1 TUBE (0168-0040-15)", "package_ndc": "0168-0040-15", "marketing_start_date": "19830831"}, {"sample": false, "description": "45 g in 1 TUBE (0168-0040-46)", "package_ndc": "0168-0040-46", "marketing_start_date": "19830831"}], "brand_name": "Betamethasone Valerate", "product_id": "0168-0040_41e96a74-4120-436e-97e5-2dc62af84b2a", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0168-0040", "generic_name": "betamethasone valerate", "labeler_name": "E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Valerate", "active_ingredients": [{"name": "BETAMETHASONE VALERATE", "strength": "1 mg/g"}], "application_number": "NDA018861", "marketing_category": "NDA", "marketing_start_date": "19830831", "listing_expiration_date": "20271231"}