Package 50090-6855-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 50090-6855-0
Digits Only 5009068550
Product NDC 50090-6855
Product ID 50090-6855_6a2bad8a-8afa-4113-bfcb-361f1cf1b901
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6855-0)

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": "6a2bad8a-8afa-4113-bfcb-361f1cf1b901", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["2343e3a1-82d0-4c70-a086-a01a0ce81ef3"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6855-0)", "package_ndc": "50090-6855-0", "marketing_start_date": "20231130"}], "brand_name": "Gabapentin", "product_id": "50090-6855_6a2bad8a-8afa-4113-bfcb-361f1cf1b901", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-6855", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA200651", "marketing_category": "ANDA", "marketing_start_date": "20111006", "listing_expiration_date": "20271231"}