tretinoin
Generic: tretinoin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
tretinoin
Generic Name
tretinoin
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
tretinoin 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-1220
Product ID
72162-1220_f882a775-5ca1-4aeb-868e-ab77e0f31875
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201687
Listing Expiration
2026-12-31
Marketing Start
2012-10-24
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721621220
Hyphenated Format
72162-1220
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
ANDA201687 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (72162-1220-1)
- 30 CAPSULE in 1 BOTTLE (72162-1220-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f882a775-5ca1-4aeb-868e-ab77e0f31875", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["199159"], "spl_set_id": ["7a7974c7-8b6c-41ae-9a48-a08a1439087a"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-1220-1)", "package_ndc": "72162-1220-1", "marketing_start_date": "20240209"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72162-1220-3)", "package_ndc": "72162-1220-3", "marketing_start_date": "20240209"}], "brand_name": "Tretinoin", "product_id": "72162-1220_f882a775-5ca1-4aeb-868e-ab77e0f31875", "dosage_form": "CAPSULE", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "72162-1220", "generic_name": "Tretinoin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": "10 mg/1"}], "application_number": "ANDA201687", "marketing_category": "ANDA", "marketing_start_date": "20121024", "listing_expiration_date": "20261231"}