betamethasone dipropionate

Generic: betamethasone dipropionate

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name betamethasone dipropionate
Generic Name betamethasone dipropionate
Labeler aurobindo pharma limited
Dosage Form OINTMENT, AUGMENTED
Routes
TOPICAL
Active Ingredients

betamethasone dipropionate .5 mg/g

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-699
Product ID 59651-699_a0864f4e-0abe-4f31-8242-b339deb69f3a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218289
Listing Expiration 2026-12-31
Marketing Start 2024-04-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651699
Hyphenated Format 59651-699

Supplemental Identifiers

RxCUI
848180
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 ANDA218289 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (59651-699-14) / 15 g in 1 TUBE
  • 1 TUBE in 1 CARTON (59651-699-46) / 45 g in 1 TUBE
  • 1 TUBE in 1 CARTON (59651-699-50) / 50 g in 1 TUBE
source: ndc

Packages (3)

59651-699-14 1 TUBE in 1 CARTON (59651-699-14) / 15 g in 1 TUBE 59651-699-46 1 TUBE in 1 CARTON (59651-699-46) / 45 g in 1 TUBE 59651-699-50 1 TUBE in 1 CARTON (59651-699-50) / 50 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": "a0864f4e-0abe-4f31-8242-b339deb69f3a", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848180"], "spl_set_id": ["e0e0baea-1744-4708-bda7-4ab7783a3fb4"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (59651-699-14)  / 15 g in 1 TUBE", "package_ndc": "59651-699-14", "marketing_start_date": "20240410"}, {"sample": false, "description": "1 TUBE in 1 CARTON (59651-699-46)  / 45 g in 1 TUBE", "package_ndc": "59651-699-46", "marketing_start_date": "20240410"}, {"sample": false, "description": "1 TUBE in 1 CARTON (59651-699-50)  / 50 g in 1 TUBE", "package_ndc": "59651-699-50", "marketing_start_date": "20240410"}], "brand_name": "BETAMETHASONE DIPROPIONATE", "product_id": "59651-699_a0864f4e-0abe-4f31-8242-b339deb69f3a", "dosage_form": "OINTMENT, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "59651-699", "generic_name": "BETAMETHASONE DIPROPIONATE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BETAMETHASONE DIPROPIONATE", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA218289", "marketing_category": "ANDA", "marketing_start_date": "20240410", "listing_expiration_date": "20261231"}