gabapentin

Generic: gabapentin

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler zydus lifesciences limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

gabapentin 800 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 65841-706
Product ID 65841-706_e9f9a5e6-0454-4601-90e4-b170bb325eb6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078926
Listing Expiration 2026-12-31
Marketing Start 2012-10-16

Pharmacologic Class

Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65841706
Hyphenated Format 65841-706

Supplemental Identifiers

RxCUI
310433 310434
UPC
0365841705010
UNII
6CW7F3G59X
NUI
N0000008486

Packaging Origin

Original Packager
true

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 ANDA078926 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (65841-706-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (65841-706-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (65841-706-10)
  • 10 BLISTER PACK in 1 CARTON (65841-706-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (4)

65841-706-01 100 TABLET, FILM COATED in 1 BOTTLE (65841-706-01) 65841-706-05 500 TABLET, FILM COATED in 1 BOTTLE (65841-706-05) 65841-706-10 1000 TABLET, FILM COATED in 1 BOTTLE (65841-706-10) 65841-706-77 10 BLISTER PACK in 1 CARTON (65841-706-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

gabapentin (800 mg/1)

Linked Drug Pages (1)

Gabapentin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e9f9a5e6-0454-4601-90e4-b170bb325eb6", "openfda": {"nui": ["N0000008486"], "upc": ["0365841705010"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["b033c169-4943-4ad9-ace0-7e4a1f0dc100"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65841-706-01)", "package_ndc": "65841-706-01", "marketing_start_date": "20121016"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65841-706-05)", "package_ndc": "65841-706-05", "marketing_start_date": "20121016"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65841-706-10)", "package_ndc": "65841-706-10", "marketing_start_date": "20121016"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65841-706-77)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65841-706-77", "marketing_start_date": "20121016"}], "brand_name": "Gabapentin", "product_id": "65841-706_e9f9a5e6-0454-4601-90e4-b170bb325eb6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "65841-706", "generic_name": "Gabapentin", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA078926", "marketing_category": "ANDA", "marketing_start_date": "20121016", "listing_expiration_date": "20261231"}