gabapentin

Generic: gabapentin

Labeler: advagen pharma ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler advagen pharma ltd
Dosage Form TABLET
Routes
ORAL
Active Ingredients

gabapentin 800 mg/1

Manufacturer
Advagen Pharma Ltd

Identifiers & Regulatory

Product NDC 72888-132
Product ID 72888-132_4b9217ba-8356-aab1-e063-6294a90a2dce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077661
Listing Expiration 2027-12-31
Marketing Start 2022-09-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72888132
Hyphenated Format 72888-132

Supplemental Identifiers

RxCUI
310433 310434
UPC
0372888132013 0372888132051 0372888132303 0372888131306 0372888131016 0372888131009 0372888132006 0372888131054
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 ANDA077661 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (72888-132-00)
  • 100 TABLET in 1 BOTTLE (72888-132-01)
  • 500 TABLET in 1 BOTTLE (72888-132-05)
  • 30 TABLET in 1 BOTTLE (72888-132-30)
source: ndc

Packages (4)

72888-132-00 1000 TABLET in 1 BOTTLE (72888-132-00) 72888-132-01 100 TABLET in 1 BOTTLE (72888-132-01) 72888-132-05 500 TABLET in 1 BOTTLE (72888-132-05) 72888-132-30 30 TABLET in 1 BOTTLE (72888-132-30)

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": "4b9217ba-8356-aab1-e063-6294a90a2dce", "openfda": {"nui": ["N0000008486"], "upc": ["0372888132013", "0372888132051", "0372888132303", "0372888131306", "0372888131016", "0372888131009", "0372888132006", "0372888131054"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["401b30fc-e143-4906-aae1-e5b5c190d4a8"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72888-132-00)", "package_ndc": "72888-132-00", "marketing_start_date": "20220922"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72888-132-01)", "package_ndc": "72888-132-01", "marketing_start_date": "20220922"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72888-132-05)", "package_ndc": "72888-132-05", "marketing_start_date": "20220922"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72888-132-30)", "package_ndc": "72888-132-30", "marketing_start_date": "20220922"}], "brand_name": "Gabapentin", "product_id": "72888-132_4b9217ba-8356-aab1-e063-6294a90a2dce", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72888-132", "generic_name": "gabapentin", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA077661", "marketing_category": "ANDA", "marketing_start_date": "20220922", "listing_expiration_date": "20271231"}