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 LOTION
Routes
TOPICAL
Active Ingredients

betamethasone dipropionate .5 mg/mL

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

Identifiers & Regulatory

Product NDC 0168-0057
Product ID 0168-0057_b3e9355b-1499-4430-9cdd-8ba0f77279c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070275
Listing Expiration 2027-12-31
Marketing Start 1985-08-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01680057
Hyphenated Format 0168-0057

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 ANDA070275 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0168-0057-60) / 60 mL in 1 BOTTLE
source: ndc

Packages (1)

0168-0057-60 1 BOTTLE in 1 CARTON (0168-0057-60) / 60 mL in 1 BOTTLE

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": "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 BOTTLE in 1 CARTON (0168-0057-60)  / 60 mL in 1 BOTTLE", "package_ndc": "0168-0057-60", "marketing_start_date": "19850812"}], "brand_name": "Betamethasone Dipropionate", "product_id": "0168-0057_b3e9355b-1499-4430-9cdd-8ba0f77279c4", "dosage_form": "LOTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0168-0057", "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/mL"}], "application_number": "ANDA070275", "marketing_category": "ANDA", "marketing_start_date": "19850812", "listing_expiration_date": "20271231"}