Package 70518-2806-2
Brand: aripiprazole
Generic: aripiprazolePackage Facts
Identity
Package NDC
70518-2806-2
Digits Only
7051828062
Product NDC
70518-2806
Description
30 TABLET in 1 BLISTER PACK (70518-2806-2)
Marketing
Marketing Status
Brand
aripiprazole
Generic
aripiprazole
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4aa33a3e-5b27-2181-e063-6294a90a838b", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349553"], "spl_set_id": ["506fa28f-6f98-4632-bce8-72a9cb507c90"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2806-2)", "package_ndc": "70518-2806-2", "marketing_start_date": "20210512"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2806-3)", "package_ndc": "70518-2806-3", "marketing_start_date": "20231207"}], "brand_name": "Aripiprazole", "product_id": "70518-2806_4aa33a3e-5b27-2181-e063-6294a90a838b", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-2806", "generic_name": "Aripiprazole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "20 mg/1"}], "application_number": "ANDA207105", "marketing_category": "ANDA", "marketing_start_date": "20200706", "listing_expiration_date": "20271231"}