tretinoin

Generic: tretinoin

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

Drug Facts

Product Profile

Brand Name tretinoin
Generic Name tretinoin
Labeler mylan pharmaceuticals inc.
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

tretinoin .5 mg/g

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 0378-8090
Product ID 0378-8090_7f967c10-776a-4b9c-aeda-70276ff2747f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207955
Listing Expiration 2026-12-31
Marketing Start 2018-11-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03788090
Hyphenated Format 0378-8090

Supplemental Identifiers

RxCUI
245723
UNII
5688UTC01R
NUI
N0000175607 M0018962

Packaging Origin

Original Packager
true

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 ANDA207955 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (0378-8090-45) / 45 g in 1 TUBE
source: ndc

Packages (1)

Ingredients (1)

tretinoin (.5 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "7f967c10-776a-4b9c-aeda-70276ff2747f", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["245723"], "spl_set_id": ["ce5f4f14-5e60-4cc1-bcb3-1fa9b8aa9cd5"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0378-8090-45)  / 45 g in 1 TUBE", "package_ndc": "0378-8090-45", "marketing_start_date": "20181114"}], "brand_name": "Tretinoin", "product_id": "0378-8090_7f967c10-776a-4b9c-aeda-70276ff2747f", "dosage_form": "GEL", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "0378-8090", "generic_name": "Tretinoin", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".5 mg/g"}], "application_number": "ANDA207955", "marketing_category": "ANDA", "marketing_start_date": "20181114", "listing_expiration_date": "20261231"}