Package 70518-2966-0
Brand: ethambutol hydrochloride
Generic: ethambutol hydrochloridePackage Facts
Identity
Package NDC
70518-2966-0
Digits Only
7051829660
Product NDC
70518-2966
Description
30 TABLET in 1 BLISTER PACK (70518-2966-0)
Marketing
Marketing Status
Brand
ethambutol hydrochloride
Generic
ethambutol hydrochloride
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4aba550b-837b-4af9-e063-6394a90af074", "openfda": {"unii": ["QE4VW5FO07"], "rxcui": ["995607"], "spl_set_id": ["c12b3482-55f0-4324-bdcd-b129ca2dae73"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2966-0)", "package_ndc": "70518-2966-0", "marketing_start_date": "20201211"}], "brand_name": "Ethambutol Hydrochloride", "product_id": "70518-2966_4aba550b-837b-4af9-e063-6394a90af074", "dosage_form": "TABLET", "pharm_class": ["Antimycobacterial [EPC]"], "product_ndc": "70518-2966", "generic_name": "Ethambutol Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ethambutol Hydrochloride", "active_ingredients": [{"name": "ETHAMBUTOL HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA078939", "marketing_category": "ANDA", "marketing_start_date": "20201211", "listing_expiration_date": "20271231"}