tretinoin

Generic: tretinoin

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

Drug Facts

Product Profile

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

tretinoin 1 mg/g

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3233
Product ID 70518-3233_3a35c95b-10e9-689f-e063-6394a90ae1d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075213
Listing Expiration 2026-12-31
Marketing Start 2021-10-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183233
Hyphenated Format 70518-3233

Supplemental Identifiers

RxCUI
198300
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 ANDA075213 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (70518-3233-0) / 20 g in 1 TUBE
source: ndc

Packages (1)

70518-3233-0 1 TUBE in 1 CARTON (70518-3233-0) / 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": "3a35c95b-10e9-689f-e063-6394a90ae1d4", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["198300"], "spl_set_id": ["c4d5155b-046d-4f94-bafc-651b572c2bd5"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (70518-3233-0)  / 20 g in 1 TUBE", "package_ndc": "70518-3233-0", "marketing_start_date": "20211011"}], "brand_name": "TRETINOIN", "product_id": "70518-3233_3a35c95b-10e9-689f-e063-6394a90ae1d4", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "70518-3233", "generic_name": "tretinoin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRETINOIN", "active_ingredients": [{"name": "TRETINOIN", "strength": "1 mg/g"}], "application_number": "ANDA075213", "marketing_category": "ANDA", "marketing_start_date": "20211011", "listing_expiration_date": "20261231"}