Package 0121-2134-40
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
0121-2134-40
Digits Only
0121213440
Product NDC
0121-2134
Description
4 TRAY in 1 CASE (0121-2134-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 6 mL in 1 CUP, UNIT-DOSE (0121-2134-06)
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": "01ef9bd4-78c9-4ec7-8633-c4e0260ad2de", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["283523"], "spl_set_id": ["6d3fd1f9-c831-4262-af10-291838a53541"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 TRAY in 1 CASE (0121-2134-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 6 mL in 1 CUP, UNIT-DOSE (0121-2134-06)", "package_ndc": "0121-2134-40", "marketing_start_date": "20250612"}], "brand_name": "Gabapentin", "product_id": "0121-2134_01ef9bd4-78c9-4ec7-8633-c4e0260ad2de", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "0121-2134", "generic_name": "Gabapentin", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "250 mg/5mL"}], "application_number": "ANDA211330", "marketing_category": "ANDA", "marketing_start_date": "20250612", "listing_expiration_date": "20261231"}