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 .5 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6819
Product ID
50090-6819_5d95cce9-168c-4f83-820a-d4b2fd83297b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211644
Listing Expiration
2027-12-31
Marketing Start
2019-01-25
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906819
Hyphenated Format
50090-6819
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
ANDA211644 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/g
Packaging
- 1 TUBE in 1 CARTON (50090-6819-0) / 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": "5d95cce9-168c-4f83-820a-d4b2fd83297b", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["106303"], "spl_set_id": ["44be2556-1ea9-49e9-86dd-991fbcc6348d"], "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 (50090-6819-0) / 45 g in 1 TUBE", "package_ndc": "50090-6819-0", "marketing_start_date": "20231114"}], "brand_name": "Tretinoin", "product_id": "50090-6819_5d95cce9-168c-4f83-820a-d4b2fd83297b", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "50090-6819", "generic_name": "tretinoin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".5 mg/g"}], "application_number": "ANDA211644", "marketing_category": "ANDA", "marketing_start_date": "20190125", "listing_expiration_date": "20271231"}