acitretin
Generic: acitretin
Labeler: amneal pharmaceuticals of new york llcDrug Facts
Product Profile
Brand Name
acitretin
Generic Name
acitretin
Labeler
amneal pharmaceuticals of new york llc
Dosage Form
CAPSULE
Routes
Active Ingredients
acitretin 22.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0115-1752
Product ID
0115-1752_233bc68a-a24e-4f19-8477-3a11e80e68df
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202552
Listing Expiration
2026-12-31
Marketing Start
2016-01-04
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01151752
Hyphenated Format
0115-1752
Supplemental Identifiers
RxCUI
UPC
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
acitretin (source: ndc)
Generic Name
acitretin (source: ndc)
Application Number
ANDA202552 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 22.5 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE, PLASTIC (0115-1752-08)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "233bc68a-a24e-4f19-8477-3a11e80e68df", "openfda": {"nui": ["N0000175607", "M0018962"], "upc": ["0301151753082", "0301151752085"], "unii": ["LCH760E9T7"], "rxcui": ["199689", "199690", "894859", "894863"], "spl_set_id": ["85507f6c-f802-479e-bacc-624b5136d092"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (0115-1752-08)", "package_ndc": "0115-1752-08", "marketing_start_date": "20160104"}], "brand_name": "Acitretin", "product_id": "0115-1752_233bc68a-a24e-4f19-8477-3a11e80e68df", "dosage_form": "CAPSULE", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "0115-1752", "generic_name": "Acitretin", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acitretin", "active_ingredients": [{"name": "ACITRETIN", "strength": "22.5 mg/1"}], "application_number": "ANDA202552", "marketing_category": "ANDA", "marketing_start_date": "20160104", "listing_expiration_date": "20261231"}