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 50090-6787
Product ID 50090-6787_df2bb243-63e3-4bfa-9c0e-f56afbd03d39
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209106
Listing Expiration 2026-12-31
Marketing Start 2020-03-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906787
Hyphenated Format 50090-6787

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 ANDA209106 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (50090-6787-0) / 50 g in 1 TUBE
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": "df2bb243-63e3-4bfa-9c0e-f56afbd03d39", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848180"], "spl_set_id": ["b5291e39-40a0-4362-9281-97f5fb4025d9"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (50090-6787-0)  / 50 g in 1 TUBE", "package_ndc": "50090-6787-0", "marketing_start_date": "20231031"}], "brand_name": "Betamethasone dipropionate", "product_id": "50090-6787_df2bb243-63e3-4bfa-9c0e-f56afbd03d39", "dosage_form": "OINTMENT, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-6787", "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": "ANDA209106", "marketing_category": "ANDA", "marketing_start_date": "20200319", "listing_expiration_date": "20261231"}