Package 0904-6867-04

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 0904-6867-04
Digits Only 0904686704
Product NDC 0904-6867
Description

30 BLISTER PACK in 1 CARTON (0904-6867-04) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2012-10-24
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": "84e260ff-4ef4-483e-af99-8923b69f66df", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["199159"], "spl_set_id": ["045258e2-5efb-4147-bf74-4c43af04dccc"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6867-04)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6867-04", "marketing_start_date": "20121024"}], "brand_name": "Tretinoin", "product_id": "0904-6867_84e260ff-4ef4-483e-af99-8923b69f66df", "dosage_form": "CAPSULE", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "0904-6867", "generic_name": "Tretinoin", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": "10 mg/1"}], "application_number": "ANDA201687", "marketing_category": "ANDA", "marketing_start_date": "20121024", "listing_expiration_date": "20261231"}