alclometasone dipropionate

Generic: alclometasone dipropionate

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alclometasone dipropionate
Generic Name alclometasone dipropionate
Labeler sun pharmaceutical industries, inc.
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

alclometasone dipropionate .5 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-1316
Product ID 51672-1316_3c44a51b-8abe-ceae-e063-6294a90a482c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076730
Listing Expiration 2026-12-31
Marketing Start 2004-07-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516721316
Hyphenated Format 51672-1316

Supplemental Identifiers

RxCUI
855480
UPC
0351672131630 0351672131616
UNII
S56PQL4N1V

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 alclometasone dipropionate (source: ndc)
Generic Name alclometasone dipropionate (source: ndc)
Application Number ANDA076730 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51672-1316-1) / 15 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1316-3) / 60 g in 1 TUBE
  • 5 g in 1 TUBE (51672-1316-5)
  • 1 TUBE in 1 CARTON (51672-1316-6) / 45 g in 1 TUBE
source: ndc

Packages (4)

51672-1316-1 1 TUBE in 1 CARTON (51672-1316-1) / 15 g in 1 TUBE 51672-1316-3 1 TUBE in 1 CARTON (51672-1316-3) / 60 g in 1 TUBE 51672-1316-5 5 g in 1 TUBE (51672-1316-5) 51672-1316-6 1 TUBE in 1 CARTON (51672-1316-6) / 45 g in 1 TUBE

Ingredients (1)

alclometasone dipropionate (.5 mg/g)

Linked Drug Pages (1)

Alclometasone Dipropionate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3c44a51b-8abe-ceae-e063-6294a90a482c", "openfda": {"upc": ["0351672131630", "0351672131616"], "unii": ["S56PQL4N1V"], "rxcui": ["855480"], "spl_set_id": ["3b0dccd6-dee1-49dd-8c6d-82df5c7ee36c"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1316-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1316-1", "marketing_start_date": "20040729"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1316-3)  / 60 g in 1 TUBE", "package_ndc": "51672-1316-3", "marketing_start_date": "20040729"}, {"sample": false, "description": "5 g in 1 TUBE (51672-1316-5)", "package_ndc": "51672-1316-5", "marketing_start_date": "20040729"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1316-6)  / 45 g in 1 TUBE", "package_ndc": "51672-1316-6", "marketing_start_date": "20040729"}], "brand_name": "Alclometasone Dipropionate", "product_id": "51672-1316_3c44a51b-8abe-ceae-e063-6294a90a482c", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1316", "generic_name": "Alclometasone dipropionate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alclometasone Dipropionate", "active_ingredients": [{"name": "ALCLOMETASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA076730", "marketing_category": "ANDA", "marketing_start_date": "20040729", "listing_expiration_date": "20261231"}