tretinoin
Generic: tretinoin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
tretinoin
Generic Name
tretinoin
Labeler
bryant ranch prepack
Dosage Form
CREAM
Routes
Active Ingredients
tretinoin .5 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2158
Product ID
72162-2158_7acc082c-03e7-48b6-b320-e9a48401356b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075265
Listing Expiration
2026-12-31
Marketing Start
2017-04-26
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622158
Hyphenated Format
72162-2158
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
ANDA075265 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/g
Packaging
- 1 TUBE in 1 CARTON (72162-2158-2) / 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": "7acc082c-03e7-48b6-b320-e9a48401356b", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["106303"], "spl_set_id": ["8929196c-389a-4c43-843c-00fbb26a1dd9"], "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 (72162-2158-2) / 45 g in 1 TUBE", "package_ndc": "72162-2158-2", "marketing_start_date": "20231207"}], "brand_name": "TRETINOIN", "product_id": "72162-2158_7acc082c-03e7-48b6-b320-e9a48401356b", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "72162-2158", "generic_name": "tretinoin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRETINOIN", "active_ingredients": [{"name": "TRETINOIN", "strength": ".5 mg/g"}], "application_number": "ANDA075265", "marketing_category": "ANDA", "marketing_start_date": "20170426", "listing_expiration_date": "20261231"}