acitretin
Generic: acitretin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
acitretin
Generic Name
acitretin
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
acitretin 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2222
Product ID
72162-2222_6fb0eb74-3b5e-4639-a6e8-4780c1c828db
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204633
Listing Expiration
2026-12-31
Marketing Start
2015-09-16
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622222
Hyphenated Format
72162-2222
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA204633 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (72162-2222-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6fb0eb74-3b5e-4639-a6e8-4780c1c828db", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["LCH760E9T7"], "rxcui": ["199689"], "spl_set_id": ["08ce9fdd-1e84-4043-b085-91053f975b64"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72162-2222-3)", "package_ndc": "72162-2222-3", "marketing_start_date": "20240126"}], "brand_name": "ACITRETIN", "product_id": "72162-2222_6fb0eb74-3b5e-4639-a6e8-4780c1c828db", "dosage_form": "CAPSULE", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "72162-2222", "generic_name": "ACITRETIN", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ACITRETIN", "active_ingredients": [{"name": "ACITRETIN", "strength": "10 mg/1"}], "application_number": "ANDA204633", "marketing_category": "ANDA", "marketing_start_date": "20150916", "listing_expiration_date": "20261231"}