tretinoin

Generic: tretinoin

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tretinoin
Generic Name tretinoin
Labeler preferred pharmaceuticals inc.
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

tretinoin .25 mg/g

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8857
Product ID 68788-8857_fda88f47-21b3-4678-ab21-befb03035730
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215713
Listing Expiration 2026-12-31
Marketing Start 2025-04-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888857
Hyphenated Format 68788-8857

Supplemental Identifiers

RxCUI
106302
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 ANDA215713 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (68788-8857-2) / 20 g in 1 TUBE
source: ndc

Packages (1)

68788-8857-2 1 TUBE in 1 CARTON (68788-8857-2) / 20 g in 1 TUBE

Ingredients (1)

tretinoin (.25 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": "fda88f47-21b3-4678-ab21-befb03035730", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["106302"], "spl_set_id": ["fda88f47-21b3-4678-ab21-befb03035730"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68788-8857-2)  / 20 g in 1 TUBE", "package_ndc": "68788-8857-2", "marketing_start_date": "20250411"}], "brand_name": "Tretinoin", "product_id": "68788-8857_fda88f47-21b3-4678-ab21-befb03035730", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "68788-8857", "generic_name": "tretinoin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".25 mg/g"}], "application_number": "ANDA215713", "marketing_category": "ANDA", "marketing_start_date": "20250411", "listing_expiration_date": "20261231"}