tretinoin
Generic: tretinoin
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
tretinoin
Generic Name
tretinoin
Labeler
nucare pharmaceuticals,inc.
Dosage Form
CREAM
Routes
Active Ingredients
tretinoin .25 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3888
Product ID
68071-3888_3deccf47-7b95-a18a-e063-6394a90a14fb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215713
Listing Expiration
2026-12-31
Marketing Start
2023-01-05
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713888
Hyphenated Format
68071-3888
Supplemental Identifiers
RxCUI
UPC
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
ANDA215713 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .25 mg/g
Packaging
- 1 TUBE in 1 CARTON (68071-3888-2) / 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": "3deccf47-7b95-a18a-e063-6394a90a14fb", "openfda": {"nui": ["N0000175607", "M0018962"], "upc": ["0368071388824"], "unii": ["5688UTC01R"], "rxcui": ["106302"], "spl_set_id": ["3deccf35-67ad-9cbc-e063-6394a90a7ee9"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68071-3888-2) / 20 g in 1 TUBE", "package_ndc": "68071-3888-2", "marketing_start_date": "20250903"}], "brand_name": "Tretinoin", "product_id": "68071-3888_3deccf47-7b95-a18a-e063-6394a90a14fb", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "68071-3888", "generic_name": "tretinoin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".25 mg/g"}], "application_number": "ANDA215713", "marketing_category": "ANDA", "marketing_start_date": "20230105", "listing_expiration_date": "20261231"}