amcinonide

Generic: amcinonide

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

Drug Facts

Product Profile

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

amcinonide 1 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-4060
Product ID 51672-4060_31e404cb-aac7-730b-e063-6394a90afc03
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076367
Listing Expiration 2026-12-31
Marketing Start 2003-03-19

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516724060
Hyphenated Format 51672-4060

Supplemental Identifiers

RxCUI
197327 197328
UNII
423W026MA9
NUI
N0000175576 N0000175450

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 amcinonide (source: ndc)
Generic Name amcinonide (source: ndc)
Application Number ANDA076367 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51672-4060-1) / 15 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-4060-2) / 30 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-4060-3) / 60 g in 1 TUBE
source: ndc

Packages (3)

51672-4060-1 1 TUBE in 1 CARTON (51672-4060-1) / 15 g in 1 TUBE 51672-4060-2 1 TUBE in 1 CARTON (51672-4060-2) / 30 g in 1 TUBE 51672-4060-3 1 TUBE in 1 CARTON (51672-4060-3) / 60 g in 1 TUBE

Ingredients (1)

amcinonide (1 mg/g)

Linked Drug Pages (1)

Amcinonide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "31e404cb-aac7-730b-e063-6394a90afc03", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["423W026MA9"], "rxcui": ["197327", "197328"], "spl_set_id": ["ac5c3e79-52f7-434e-92ae-24bd32b45edc"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-4060-1)  / 15 g in 1 TUBE", "package_ndc": "51672-4060-1", "marketing_start_date": "20030319"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-4060-2)  / 30 g in 1 TUBE", "package_ndc": "51672-4060-2", "marketing_start_date": "20030319"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-4060-3)  / 60 g in 1 TUBE", "package_ndc": "51672-4060-3", "marketing_start_date": "20030319"}], "brand_name": "Amcinonide", "product_id": "51672-4060_31e404cb-aac7-730b-e063-6394a90afc03", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-4060", "generic_name": "Amcinonide", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amcinonide", "active_ingredients": [{"name": "AMCINONIDE", "strength": "1 mg/g"}], "application_number": "ANDA076367", "marketing_category": "ANDA", "marketing_start_date": "20030319", "listing_expiration_date": "20261231"}