Package 63187-148-90
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
63187-148-90
Digits Only
6318714890
Product NDC
63187-148
Description
90 TABLET, FILM COATED in 1 BOTTLE (63187-148-90)
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": "f55b43a8-4ccf-4b28-be7d-8850f5a17222", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["c79d94ec-117d-4fb6-845d-1954e3472bb0"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-148-90)", "package_ndc": "63187-148-90", "marketing_start_date": "20190101"}], "brand_name": "Gabapentin", "product_id": "63187-148_f55b43a8-4ccf-4b28-be7d-8850f5a17222", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "63187-148", "generic_name": "Gabapentin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA200651", "marketing_category": "ANDA", "marketing_start_date": "20111006", "listing_expiration_date": "20261231"}