betamethasone dipropionate

Generic: betamethasone dipropionate

Labeler: e. fougera & co. a division of fougera pharmaceuticals, llc
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, llc
Dosage Form LOTION, AUGMENTED
Routes
TOPICAL
Active Ingredients

betamethasone dipropionate .5 mg/mL

Manufacturer
E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 0168-0267
Product ID 0168-0267_5d745268-8539-4108-a0eb-444a4b1424b9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077111
Listing Expiration 2027-12-31
Marketing Start 2007-05-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01680267
Hyphenated Format 0168-0267

Supplemental Identifiers

RxCUI
848178
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 ANDA077111 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/mL
source: ndc
Packaging
  • 30 mL in 1 BOTTLE (0168-0267-30)
  • 60 mL in 1 BOTTLE (0168-0267-60)
source: ndc

Packages (2)

0168-0267-30 30 mL in 1 BOTTLE (0168-0267-30) 0168-0267-60 60 mL in 1 BOTTLE (0168-0267-60)

Ingredients (1)

betamethasone dipropionate (.5 mg/mL)

Linked Drug Pages (1)

Betamethasone Dipropionate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "5d745268-8539-4108-a0eb-444a4b1424b9", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848178"], "spl_set_id": ["4f411e41-00dc-47cf-8517-3ff5876e1bf5"], "manufacturer_name": ["E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (0168-0267-30)", "package_ndc": "0168-0267-30", "marketing_start_date": "20070521"}, {"sample": false, "description": "60 mL in 1 BOTTLE (0168-0267-60)", "package_ndc": "0168-0267-60", "marketing_start_date": "20070521"}], "brand_name": "Betamethasone Dipropionate", "product_id": "0168-0267_5d745268-8539-4108-a0eb-444a4b1424b9", "dosage_form": "LOTION, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0168-0267", "generic_name": "Betamethasone Dipropionate", "labeler_name": "E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/mL"}], "application_number": "ANDA077111", "marketing_category": "ANDA", "marketing_start_date": "20070521", "listing_expiration_date": "20271231"}