Package 10370-268-01

Brand: tretinoin

Generic: tretinoin
NDC Package

Package Facts

Identity

Package NDC 10370-268-01
Digits Only 1037026801
Product NDC 10370-268
Product ID 10370-268_f124fad5-1e6a-4161-bc98-2b927e2df5d2
Description

100 CAPSULE in 1 BOTTLE (10370-268-01)

Marketing

Marketing Status
Marketed Since 2012-10-24
Brand tretinoin
Generic tretinoin
Sample Package No

Linked Drug Pages (1)

Tretinoin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f124fad5-1e6a-4161-bc98-2b927e2df5d2", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["199159"], "spl_set_id": ["9c4ae9d9-c2a0-4995-a27a-e3f0f0284db9"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (10370-268-01)", "package_ndc": "10370-268-01", "marketing_start_date": "20121024"}], "brand_name": "Tretinoin", "product_id": "10370-268_f124fad5-1e6a-4161-bc98-2b927e2df5d2", "dosage_form": "CAPSULE", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "10370-268", "generic_name": "Tretinoin", "labeler_name": "Endo USA, Inc.", "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"}