tretinoin
Generic: tretinoin
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
tretinoin
Generic Name
tretinoin
Labeler
a-s medication solutions
Dosage Form
CREAM
Routes
Active Ingredients
tretinoin .25 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
50090-0651
Product ID
50090-0651_0bd4165c-feb6-4dcc-83c2-98b76944fe6e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA020404
Listing Expiration
2026-12-31
Marketing Start
1998-04-20
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500900651
Hyphenated Format
50090-0651
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
tretinoin (source: ndc)
Generic Name
tretinoin (source: ndc)
Application Number
NDA020404 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .25 mg/g
Packaging
- 1 TUBE in 1 CARTON (50090-0651-0) / 20 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": "0bd4165c-feb6-4dcc-83c2-98b76944fe6e", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["106302"], "spl_set_id": ["c7860dcd-91b0-44e0-98d6-a843b16457e1"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (50090-0651-0) / 20 g in 1 TUBE", "package_ndc": "50090-0651-0", "marketing_start_date": "20141128"}], "brand_name": "Tretinoin", "product_id": "50090-0651_0bd4165c-feb6-4dcc-83c2-98b76944fe6e", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "50090-0651", "generic_name": "Tretinoin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".25 mg/g"}], "application_number": "NDA020404", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19980420", "listing_expiration_date": "20261231"}