Package 68682-800-45

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 68682-800-45
Digits Only 6868280045
Product NDC 68682-800
Description

1 TUBE in 1 PACKAGE (68682-800-45) / 45 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2007-07-26
Brand tretinoin
Generic tretinoin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "465e7164-5e77-4a2b-ae94-6ea7966af0e5", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["245723"], "spl_set_id": ["febda58b-c9ee-4b95-bee7-dca5f2645f98"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 PACKAGE (68682-800-45)  / 45 g in 1 TUBE", "package_ndc": "68682-800-45", "marketing_start_date": "20070726"}], "brand_name": "Tretinoin", "product_id": "68682-800_465e7164-5e77-4a2b-ae94-6ea7966af0e5", "dosage_form": "GEL", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "68682-800", "generic_name": "Tretinoin", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".05 g/100g"}], "application_number": "NDA022070", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20070726", "listing_expiration_date": "20261231"}