Package 81033-124-44
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
81033-124-44
Digits Only
8103312444
Product NDC
81033-124
Description
40 CUP, UNIT-DOSE in 1 CARTON (81033-124-44) / 6 mL in 1 CUP, UNIT-DOSE (81033-124-06)
Marketing
Marketing Status
Brand
gabapentin
Generic
gabapentin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f2ba3d6-6087-eaf2-e063-6294a90a7642", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["283523"], "spl_set_id": ["3f2ba3d6-6086-eaf2-e063-6294a90a7642"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Kesin Pharma Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "40 CUP, UNIT-DOSE in 1 CARTON (81033-124-44) / 6 mL in 1 CUP, UNIT-DOSE (81033-124-06)", "package_ndc": "81033-124-44", "marketing_start_date": "20250901"}], "brand_name": "Gabapentin", "product_id": "81033-124_3f2ba3d6-6087-eaf2-e063-6294a90a7642", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "81033-124", "generic_name": "Gabapentin", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "50 mg/mL"}], "application_number": "ANDA091286", "marketing_category": "ANDA", "marketing_start_date": "20250806", "listing_expiration_date": "20261231"}