tretinoin
Generic: tretinoin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
tretinoin
Generic Name
tretinoin
Labeler
bryant ranch prepack
Dosage Form
GEL
Routes
Active Ingredients
tretinoin .25 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2898
Product ID
71335-2898_ca82745d-d880-4b6a-af76-97b8ce1519ab
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA017579
Listing Expiration
2026-12-31
Marketing Start
2019-07-12
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352898
Hyphenated Format
71335-2898
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
NDA017579 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .25 mg/g
Packaging
- 1 TUBE in 1 CARTON (71335-2898-1) / 45 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": "ca82745d-d880-4b6a-af76-97b8ce1519ab", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["313451"], "spl_set_id": ["a1ae0000-3411-47e5-94f2-ae2ee70eadfb"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (71335-2898-1) / 45 g in 1 TUBE", "package_ndc": "71335-2898-1", "marketing_start_date": "20251021"}], "brand_name": "Tretinoin", "product_id": "71335-2898_ca82745d-d880-4b6a-af76-97b8ce1519ab", "dosage_form": "GEL", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "71335-2898", "generic_name": "Tretinoin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".25 mg/g"}], "application_number": "NDA017579", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190712", "listing_expiration_date": "20261231"}