gabapentin
Generic: gabapentin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
gabapentin
Generic Name
gabapentin
Labeler
bryant ranch prepack
Dosage Form
SOLUTION
Routes
Active Ingredients
gabapentin 250 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
72162-1318
Product ID
72162-1318_a80b1881-b000-4369-ba1d-74058977324f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076403
Listing Expiration
2026-12-31
Marketing Start
2012-10-01
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721621318
Hyphenated Format
72162-1318
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
gabapentin (source: ndc)
Generic Name
gabapentin (source: ndc)
Application Number
ANDA076403 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/5mL
Packaging
- 470 mL in 1 BOTTLE (72162-1318-4)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a80b1881-b000-4369-ba1d-74058977324f", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["283523"], "spl_set_id": ["5134369d-c7f6-4569-a425-d50e5a5d694f"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "470 mL in 1 BOTTLE (72162-1318-4)", "package_ndc": "72162-1318-4", "marketing_start_date": "20241101"}], "brand_name": "Gabapentin", "product_id": "72162-1318_a80b1881-b000-4369-ba1d-74058977324f", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72162-1318", "generic_name": "gabapentin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "250 mg/5mL"}], "application_number": "ANDA076403", "marketing_category": "ANDA", "marketing_start_date": "20121001", "listing_expiration_date": "20261231"}