betamethasone dipropionate

Generic: betamethasone dipropionate

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

Drug Facts

Product Profile

Brand Name betamethasone dipropionate
Generic Name betamethasone dipropionate
Labeler e. fougera & co. a division of fougera pharmaceuticals inc.
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

betamethasone dipropionate .5 mg/g

Manufacturer
E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 0168-0056
Product ID 0168-0056_b3e9355b-1499-4430-9cdd-8ba0f77279c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019141
Listing Expiration 2027-12-31
Marketing Start 1984-09-04

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01680056
Hyphenated Format 0168-0056

Supplemental Identifiers

RxCUI
197405 238920 240209
UPC
0301680055466 0301680056159
UNII
826Y60901U

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 dipropionate (source: ndc)
Generic Name betamethasone dipropionate (source: ndc)
Application Number NDA019141 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (0168-0056-15) / 15 g in 1 TUBE
  • 1 TUBE in 1 CARTON (0168-0056-46) / 45 g in 1 TUBE
source: ndc

Packages (2)

0168-0056-15 1 TUBE in 1 CARTON (0168-0056-15) / 15 g in 1 TUBE 0168-0056-46 1 TUBE in 1 CARTON (0168-0056-46) / 45 g in 1 TUBE

Ingredients (1)

betamethasone dipropionate (.5 mg/g)

Linked Drug Pages (1)

Betamethasone Dipropionate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "b3e9355b-1499-4430-9cdd-8ba0f77279c4", "openfda": {"upc": ["0301680055466", "0301680056159"], "unii": ["826Y60901U"], "rxcui": ["197405", "238920", "240209"], "spl_set_id": ["97dde5f5-a865-4af2-b562-8da72c8475f3"], "manufacturer_name": ["E. Fougera & Co. a division of Fougera Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0168-0056-15)  / 15 g in 1 TUBE", "package_ndc": "0168-0056-15", "marketing_start_date": "19840904"}, {"sample": false, "description": "1 TUBE in 1 CARTON (0168-0056-46)  / 45 g in 1 TUBE", "package_ndc": "0168-0056-46", "marketing_start_date": "19840904"}], "brand_name": "Betamethasone Dipropionate", "product_id": "0168-0056_b3e9355b-1499-4430-9cdd-8ba0f77279c4", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0168-0056", "generic_name": "Betamethasone Dipropionate", "labeler_name": "E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "NDA019141", "marketing_category": "NDA", "marketing_start_date": "19840904", "listing_expiration_date": "20271231"}