Package 70518-2674-0

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 70518-2674-0
Digits Only 7051826740
Product NDC 70518-2674
Product ID 70518-2674_4a7d4fb2-bc97-2031-e063-6294a90a2a5d
Description

100 POUCH in 1 BOX (70518-2674-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2674-1)

Marketing

Marketing Status
Marketed Since 2020-04-06
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a7d4fb2-bc97-2031-e063-6294a90a2a5d", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["ed24bb3a-bba1-4b27-8733-96619793fc15"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2674-0)  / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2674-1)", "package_ndc": "70518-2674-0", "marketing_start_date": "20200406"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2674-2)", "package_ndc": "70518-2674-2", "marketing_start_date": "20210430"}], "brand_name": "Divalproex Sodium", "product_id": "70518-2674_4a7d4fb2-bc97-2031-e063-6294a90a2a5d", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70518-2674", "generic_name": "Divalproex Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA078597", "marketing_category": "ANDA", "marketing_start_date": "20200406", "listing_expiration_date": "20271231"}