Package 50090-7169-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 50090-7169-0
Digits Only 5009071690
Product NDC 50090-7169
Product ID 50090-7169_90f2a197-f9d9-4c5d-9897-26e5ec53c9b4
Description

90 CAPSULE in 1 BOTTLE (50090-7169-0)

Marketing

Marketing Status
Marketed Since 2024-05-14
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "90f2a197-f9d9-4c5d-9897-26e5ec53c9b4", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["c979f80b-d4b1-40f7-b878-b216db5f325d"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-7169-0)", "package_ndc": "50090-7169-0", "marketing_start_date": "20240514"}], "brand_name": "Gabapentin", "product_id": "50090-7169_90f2a197-f9d9-4c5d-9897-26e5ec53c9b4", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7169", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA090858", "marketing_category": "ANDA", "marketing_start_date": "20110129", "listing_expiration_date": "20271231"}