calcipotriene and betamethasone dipropionate (51672-1402)

Drug Facts

Product Profile

Brand Name calcipotriene and betamethasone dipropionate

Generic Name calcipotriene and betamethasone dipropionate

Labeler sun pharmaceutical industries, inc.

Dosage Form SUSPENSION

Routes

TOPICAL

Active Ingredients

betamethasone dipropionate 50 mg/g, calcipotriene 50 ug/g

Manufacturer

Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-1402

Product ID 51672-1402_38e5b828-cecd-c95b-e063-6394a90ae2e0

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA213269

Listing Expiration 2026-12-31

Marketing Start 2020-09-02

Pharmacologic Class

Established (EPC)

vitamin d analog [epc]

Chemical Structure

vitamin d [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516721402

Hyphenated Format 51672-1402

Supplemental Identifiers

UNII

826Y60901U 143NQ3779B

NUI

M0022797 N0000175849

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 calcipotriene and betamethasone dipropionate (source: ndc)

Generic Name calcipotriene and betamethasone dipropionate (source: ndc)

Application Number ANDA213269 (source: ndc)

Routes

TOPICAL

source: ndc

Resolved Composition

Strengths

50 mg/g
50 ug/g

source: ndc

Packaging

1 BOTTLE in 1 CARTON (51672-1402-4) / 60 g in 1 BOTTLE
2 BOTTLE in 1 CARTON (51672-1402-8) / 60 g in 1 BOTTLE

source: ndc

Packages (2)

51672-1402-4 1 BOTTLE in 1 CARTON (51672-1402-4) / 60 g in 1 BOTTLE 51672-1402-8 2 BOTTLE in 1 CARTON (51672-1402-8) / 60 g in 1 BOTTLE

Ingredients (2)

betamethasone dipropionate (50 mg/g) calcipotriene (50 ug/g)

Linked Drug Pages (1)

Calcipotriene and Betamethasone Dipropionate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["TOPICAL"], "spl_id": "38e5b828-cecd-c95b-e063-6394a90ae2e0", "openfda": {"nui": ["M0022797", "N0000175849"], "unii": ["826Y60901U", "143NQ3779B"], "spl_set_id": ["1d0ab2e6-1ab1-4d3e-ad55-7fa26446f191"], "pharm_class_cs": ["Vitamin D [CS]"], "pharm_class_epc": ["Vitamin D Analog [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-1402-4)  / 60 g in 1 BOTTLE", "package_ndc": "51672-1402-4", "marketing_start_date": "20200902"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (51672-1402-8)  / 60 g in 1 BOTTLE", "package_ndc": "51672-1402-8", "marketing_start_date": "20200902"}], "brand_name": "Calcipotriene and Betamethasone Dipropionate", "product_id": "51672-1402_38e5b828-cecd-c95b-e063-6394a90ae2e0", "dosage_form": "SUSPENSION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "Vitamin D Analog [EPC]", "Vitamin D [CS]"], "product_ndc": "51672-1402", "generic_name": "Calcipotriene and Betamethasone Dipropionate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Calcipotriene and Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": "50 mg/g"}, {"name": "CALCIPOTRIENE", "strength": "50 ug/g"}], "application_number": "ANDA213269", "marketing_category": "ANDA", "marketing_start_date": "20200902", "listing_expiration_date": "20261231"}