Package 68462-792-01

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 68462-792-01
Digits Only 6846279201
Product NDC 68462-792
Description

100 CAPSULE in 1 BOTTLE (68462-792-01)

Marketing

Marketing Status
Marketed Since 2016-12-23
Brand tretinoin
Generic tretinoin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5761f729-3e1f-4fe7-9d5f-cfb652bf1625", "openfda": {"nui": ["N0000175607", "M0018962"], "upc": ["0368462792018"], "unii": ["5688UTC01R"], "rxcui": ["199159"], "spl_set_id": ["264138c1-9e5f-45ef-be87-79ca97c989d9"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68462-792-01)", "package_ndc": "68462-792-01", "marketing_start_date": "20161223"}], "brand_name": "Tretinoin", "product_id": "68462-792_5761f729-3e1f-4fe7-9d5f-cfb652bf1625", "dosage_form": "CAPSULE", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "68462-792", "generic_name": "Tretinoin", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": "10 mg/1"}], "application_number": "ANDA208279", "marketing_category": "ANDA", "marketing_start_date": "20161223", "listing_expiration_date": "20271231"}