Package 44523-120-16

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 44523-120-16
Digits Only 4452312016
Product NDC 44523-120
Product ID 44523-120_462c7cf4-92a8-cf81-e063-6294a90a43c3
Description

470 mL in 1 BOTTLE (44523-120-16)

Marketing

Marketing Status
Marketed Since 2023-11-30
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (1)

Gabapentin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "462c7cf4-92a8-cf81-e063-6294a90a43c3", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["283523"], "spl_set_id": ["0b3a4009-42f3-c84f-e063-6294a90a8068"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["BioComp Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "470 mL in 1 BOTTLE (44523-120-16)", "package_ndc": "44523-120-16", "marketing_start_date": "20231130"}], "brand_name": "Gabapentin", "product_id": "44523-120_462c7cf4-92a8-cf81-e063-6294a90a43c3", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "44523-120", "generic_name": "Gabapentin", "labeler_name": "BioComp Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "250 mg/5mL"}], "application_number": "ANDA078974", "marketing_category": "ANDA", "marketing_start_date": "20231130", "listing_expiration_date": "20261231"}