betamethasone dipropionate

Generic: betamethasone dipropionate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name betamethasone dipropionate
Generic Name betamethasone dipropionate
Labeler a-s medication solutions
Dosage Form OINTMENT, AUGMENTED
Routes
TOPICAL
Active Ingredients

betamethasone dipropionate .5 mg/g

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7517
Product ID 50090-7517_3140f140-758c-41a6-83e2-8cb9be901863
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075373
Listing Expiration 2026-12-31
Marketing Start 1999-06-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907517
Hyphenated Format 50090-7517

Supplemental Identifiers

RxCUI
848180
UNII
826Y60901U

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 dipropionate (source: ndc)
Generic Name betamethasone dipropionate (source: ndc)
Application Number ANDA075373 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/g
source: ndc
Packaging
  • 50 g in 1 TUBE (50090-7517-0)
source: ndc

Packages (1)

Ingredients (1)

betamethasone dipropionate (.5 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3140f140-758c-41a6-83e2-8cb9be901863", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848180"], "spl_set_id": ["018fcec3-bfb4-451c-9b54-d1fd389c2a44"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 TUBE (50090-7517-0)", "package_ndc": "50090-7517-0", "marketing_start_date": "20250311"}], "brand_name": "Betamethasone Dipropionate", "product_id": "50090-7517_3140f140-758c-41a6-83e2-8cb9be901863", "dosage_form": "OINTMENT, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-7517", "generic_name": "betamethasone dipropionate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA075373", "marketing_category": "ANDA", "marketing_start_date": "19990622", "listing_expiration_date": "20261231"}