betamethasone dipropionate

Generic: betamethasone dipropionate

Labeler: e. fougera & co. a division of fougera pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA 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, AUGMENTED
Routes
TOPICAL
Active Ingredients

betamethasone dipropionate .5 mg/g

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

Identifiers & Regulatory

Product NDC 0168-0268
Product ID 0168-0268_e6484210-45ae-49f9-9b3a-ff7b309e9bc9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075373
Listing Expiration 2027-12-31
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 01680268
Hyphenated Format 0168-0268

Supplemental Identifiers

RxCUI
848180
UPC
0301680268156
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 ANDA075373 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/g
source: ndc
Packaging
  • 15 g in 1 TUBE (0168-0268-15)
  • 50 g in 1 TUBE (0168-0268-50)
source: ndc

Packages (2)

0168-0268-15 15 g in 1 TUBE (0168-0268-15) 0168-0268-50 50 g in 1 TUBE (0168-0268-50)

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": "e6484210-45ae-49f9-9b3a-ff7b309e9bc9", "openfda": {"upc": ["0301680268156"], "unii": ["826Y60901U"], "rxcui": ["848180"], "spl_set_id": ["853399f8-95a7-41f3-80e7-7ed8e3ff1a5e"], "manufacturer_name": ["E. Fougera & Co. a division of Fougera Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 g in 1 TUBE (0168-0268-15)", "package_ndc": "0168-0268-15", "marketing_start_date": "19990622"}, {"sample": false, "description": "50 g in 1 TUBE (0168-0268-50)", "package_ndc": "0168-0268-50", "marketing_start_date": "19990622"}], "brand_name": "Betamethasone Dipropionate", "product_id": "0168-0268_e6484210-45ae-49f9-9b3a-ff7b309e9bc9", "dosage_form": "OINTMENT, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0168-0268", "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": "ANDA075373", "marketing_category": "ANDA", "marketing_start_date": "19990622", "listing_expiration_date": "20271231"}