tretinoin

Generic: tretinoin

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name tretinoin
Generic Name tretinoin
Labeler bryant ranch prepack
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

tretinoin .1 mg/g

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2952
Product ID 71335-2952_8f5850a4-4294-418c-8b1f-65f229e5973f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA017955
Listing Expiration 2026-12-31
Marketing Start 2019-08-12

Pharmacologic Class

Established (EPC)
retinoid [epc]
Chemical Structure
retinoids [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352952
Hyphenated Format 71335-2952

Supplemental Identifiers

RxCUI
313450
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 NDA017955 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (71335-2952-1) / 45 g in 1 TUBE
source: ndc

Packages (1)

71335-2952-1 1 TUBE in 1 CARTON (71335-2952-1) / 45 g in 1 TUBE

Ingredients (1)

tretinoin (.1 mg/g)

Linked Drug Pages (1)

Tretinoin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "8f5850a4-4294-418c-8b1f-65f229e5973f", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["313450"], "spl_set_id": ["04f14d6e-5b44-44bd-a7f3-d684d9c5d7cb"], "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 (71335-2952-1)  / 45 g in 1 TUBE", "package_ndc": "71335-2952-1", "marketing_start_date": "20251021"}], "brand_name": "Tretinoin", "product_id": "71335-2952_8f5850a4-4294-418c-8b1f-65f229e5973f", "dosage_form": "GEL", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "71335-2952", "generic_name": "Tretinoin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".1 mg/g"}], "application_number": "NDA017955", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190812", "listing_expiration_date": "20261231"}