tretinoin

Generic: tretinoin

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

Drug Facts

Product Profile

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

tretinoin 1 mg/g

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3826
Product ID 68071-3826_31d2cd0d-3cb4-c719-e063-6294a90a2eb3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211645
Listing Expiration 2026-12-31
Marketing Start 2019-01-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713826
Hyphenated Format 68071-3826

Supplemental Identifiers

RxCUI
198300
UPC
0368071382624
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 ANDA211645 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (68071-3826-2) / 20 g in 1 TUBE
source: ndc

Packages (1)

68071-3826-2 1 TUBE in 1 CARTON (68071-3826-2) / 20 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": "31d2cd0d-3cb4-c719-e063-6294a90a2eb3", "openfda": {"nui": ["N0000175607", "M0018962"], "upc": ["0368071382624"], "unii": ["5688UTC01R"], "rxcui": ["198300"], "spl_set_id": ["31d2cd00-e534-6755-e063-6394a90ab8bb"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68071-3826-2)  / 20 g in 1 TUBE", "package_ndc": "68071-3826-2", "marketing_start_date": "20250402"}], "brand_name": "Tretinoin", "product_id": "68071-3826_31d2cd0d-3cb4-c719-e063-6294a90a2eb3", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "68071-3826", "generic_name": "tretinoin", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": "1 mg/g"}], "application_number": "ANDA211645", "marketing_category": "ANDA", "marketing_start_date": "20190122", "listing_expiration_date": "20261231"}