tazarotene
Generic: tazarotene
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
tazarotene
Generic Name
tazarotene
Labeler
sun pharmaceutical industries, inc.
Dosage Form
CREAM
Routes
Active Ingredients
tazarotene 1 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
51672-1374
Product ID
51672-1374_39620f25-787e-f51b-e063-6294a90a36de
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208258
Listing Expiration
2026-12-31
Marketing Start
2017-04-03
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516721374
Hyphenated Format
51672-1374
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
tazarotene (source: ndc)
Generic Name
tazarotene (source: ndc)
Application Number
ANDA208258 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/g
Packaging
- 1 TUBE in 1 CARTON (51672-1374-2) / 30 g in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "39620f25-787e-f51b-e063-6294a90a36de", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["81BDR9Y8PS"], "rxcui": ["313200"], "spl_set_id": ["34d79c31-1568-4797-a4f5-31200c7788db"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1374-2) / 30 g in 1 TUBE", "package_ndc": "51672-1374-2", "marketing_start_date": "20170403"}], "brand_name": "Tazarotene", "product_id": "51672-1374_39620f25-787e-f51b-e063-6294a90a36de", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "51672-1374", "generic_name": "Tazarotene", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tazarotene", "active_ingredients": [{"name": "TAZAROTENE", "strength": "1 mg/g"}], "application_number": "ANDA208258", "marketing_category": "ANDA", "marketing_start_date": "20170403", "listing_expiration_date": "20261231"}