Package 0116-4021-11

Brand: valproic acid

Generic: valproic acid
NDC Package

Package Facts

Identity

Package NDC 0116-4021-11
Digits Only 0116402111
Product NDC 0116-4021
Description

10 TRAY in 1 CASE (0116-4021-11) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0116-4021-10)

Marketing

Marketing Status
Marketed Since 2025-07-29
Brand valproic acid
Generic valproic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b124fef-0b53-8f72-e063-6394a90a81c4", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751"], "unii": ["614OI1Z5WI"], "rxcui": ["1099687"], "spl_set_id": ["3b124a29-30bd-d30e-e063-6294a90ac4ca"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]", "Mood Stabilizer [EPC]"], "manufacturer_name": ["Xttrium Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (0116-4021-11)  / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0116-4021-10)", "package_ndc": "0116-4021-11", "marketing_start_date": "20250729"}, {"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (0116-4021-16)", "package_ndc": "0116-4021-16", "marketing_start_date": "20250729"}, {"sample": false, "description": "4 TRAY in 1 CASE (0116-4021-40)  / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0116-4021-05)", "package_ndc": "0116-4021-40", "marketing_start_date": "20250729"}, {"sample": false, "description": "10 TRAY in 1 CASE (0116-4021-41)  / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0116-4021-05)", "package_ndc": "0116-4021-41", "marketing_start_date": "20250729"}], "brand_name": "Valproic Acid", "product_id": "0116-4021_3b124fef-0b53-8f72-e063-6394a90a81c4", "dosage_form": "SOLUTION", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "0116-4021", "generic_name": "Valproic Acid", "labeler_name": "Xttrium Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valproic Acid", "active_ingredients": [{"name": "VALPROIC ACID", "strength": "250 mg/5mL"}], "application_number": "ANDA070868", "marketing_category": "ANDA", "marketing_start_date": "19860701", "listing_expiration_date": "20261231"}