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 600 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1026
Product ID
71335-1026_db7c39b3-ffdf-452c-b42e-f4be1b60c638
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203244
Listing Expiration
2026-12-31
Marketing Start
2014-01-11
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351026
Hyphenated Format
71335-1026
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
ANDA203244 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 600 mg/1
Packaging
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1026-1)
- 58 TABLET, FILM COATED in 1 BOTTLE (71335-1026-2)
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-1026-3)
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-1026-4)
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1026-5)
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1026-6)
Packages (6)
71335-1026-1
90 TABLET, FILM COATED in 1 BOTTLE (71335-1026-1)
71335-1026-2
58 TABLET, FILM COATED in 1 BOTTLE (71335-1026-2)
71335-1026-3
100 TABLET, FILM COATED in 1 BOTTLE (71335-1026-3)
71335-1026-4
120 TABLET, FILM COATED in 1 BOTTLE (71335-1026-4)
71335-1026-5
60 TABLET, FILM COATED in 1 BOTTLE (71335-1026-5)
71335-1026-6
30 TABLET, FILM COATED in 1 BOTTLE (71335-1026-6)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "db7c39b3-ffdf-452c-b42e-f4be1b60c638", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["6e6b9d8f-9f9e-4760-96ea-fb8b0a3bbbdb"], "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 (71335-1026-1)", "package_ndc": "71335-1026-1", "marketing_start_date": "20181213"}, {"sample": false, "description": "58 TABLET, FILM COATED in 1 BOTTLE (71335-1026-2)", "package_ndc": "71335-1026-2", "marketing_start_date": "20240402"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1026-3)", "package_ndc": "71335-1026-3", "marketing_start_date": "20190911"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-1026-4)", "package_ndc": "71335-1026-4", "marketing_start_date": "20190314"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1026-5)", "package_ndc": "71335-1026-5", "marketing_start_date": "20190111"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1026-6)", "package_ndc": "71335-1026-6", "marketing_start_date": "20190130"}], "brand_name": "Gabapentin", "product_id": "71335-1026_db7c39b3-ffdf-452c-b42e-f4be1b60c638", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-1026", "generic_name": "GABAPENTIN", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA203244", "marketing_category": "ANDA", "marketing_start_date": "20140111", "listing_expiration_date": "20261231"}