tretinoin

Generic: tretinoin

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tretinoin
Generic Name tretinoin
Labeler bryant ranch prepack
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tretinoin 10 mg/1

Manufacturer
Bryant Ranch Prepack

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)
retinoid [epc]
Chemical Structure
retinoids [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721621220
Hyphenated Format 72162-1220

Supplemental Identifiers

RxCUI
199159
UNII
5688UTC01R
NUI
N0000175607 M0018962

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (72162-1220-1)
  • 30 CAPSULE in 1 BOTTLE (72162-1220-3)
source: ndc

Packages (2)

Ingredients (1)

tretinoin (10 mg/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"}