betamethasone dipropionate
Generic: betamethasone dipropionate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
betamethasone dipropionate
Generic Name
betamethasone dipropionate
Labeler
a-s medication solutions
Dosage Form
OINTMENT, AUGMENTED
Routes
Active Ingredients
betamethasone dipropionate .5 mg/g
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906787
Hyphenated Format
50090-6787
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- .5 mg/g
Packaging
- 1 TUBE in 1 CARTON (50090-6787-0) / 50 g in 1 TUBE
Packages (1)
Ingredients (1)
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"}