gabapentin
Generic: gabapentin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
gabapentin
Generic Name
gabapentin
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
gabapentin 800 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2819
Product ID
71335-2819_08d539a0-e23e-468e-abb3-2617ec34c112
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200651
Listing Expiration
2026-12-31
Marketing Start
2011-10-06
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352819
Hyphenated Format
71335-2819
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
ANDA200651 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 800 mg/1
Packaging
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-2819-1)
- 18 TABLET, FILM COATED in 1 BOTTLE (71335-2819-2)
- 58 TABLET, FILM COATED in 1 BOTTLE (71335-2819-3)
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-2819-4)
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-2819-5)
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-2819-6)
Packages (6)
71335-2819-1
90 TABLET, FILM COATED in 1 BOTTLE (71335-2819-1)
71335-2819-2
18 TABLET, FILM COATED in 1 BOTTLE (71335-2819-2)
71335-2819-3
58 TABLET, FILM COATED in 1 BOTTLE (71335-2819-3)
71335-2819-4
60 TABLET, FILM COATED in 1 BOTTLE (71335-2819-4)
71335-2819-5
30 TABLET, FILM COATED in 1 BOTTLE (71335-2819-5)
71335-2819-6
120 TABLET, FILM COATED in 1 BOTTLE (71335-2819-6)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "08d539a0-e23e-468e-abb3-2617ec34c112", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["d9d78138-e1e9-4107-9099-4910cb1422d8"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2819-1)", "package_ndc": "71335-2819-1", "marketing_start_date": "20251022"}, {"sample": false, "description": "18 TABLET, FILM COATED in 1 BOTTLE (71335-2819-2)", "package_ndc": "71335-2819-2", "marketing_start_date": "20251022"}, {"sample": false, "description": "58 TABLET, FILM COATED in 1 BOTTLE (71335-2819-3)", "package_ndc": "71335-2819-3", "marketing_start_date": "20251022"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2819-4)", "package_ndc": "71335-2819-4", "marketing_start_date": "20251022"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2819-5)", "package_ndc": "71335-2819-5", "marketing_start_date": "20251022"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2819-6)", "package_ndc": "71335-2819-6", "marketing_start_date": "20251022"}], "brand_name": "Gabapentin", "product_id": "71335-2819_08d539a0-e23e-468e-abb3-2617ec34c112", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-2819", "generic_name": "Gabapentin", "labeler_name": "Bryant Ranch Prepack", "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"}