gabapentin

Generic: gabapentin

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

gabapentin 800 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-518
Product ID 60687-518_37dcca50-b1a8-24e7-e063-6394a90a8adf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078926
Listing Expiration 2026-12-31
Marketing Start 2020-03-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687518
Hyphenated Format 60687-518

Supplemental Identifiers

RxCUI
310433 310434
UNII
6CW7F3G59X
NUI
N0000008486

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 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-518-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-518-11)
source: ndc

Packages (1)

60687-518-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-518-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-518-11)

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": "37dcca50-b1a8-24e7-e063-6394a90a8adf", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["765c7ce0-bbf5-4265-8ff0-1ba092c69865"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-518-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-518-11)", "package_ndc": "60687-518-01", "marketing_start_date": "20200302"}], "brand_name": "Gabapentin", "product_id": "60687-518_37dcca50-b1a8-24e7-e063-6394a90a8adf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "60687-518", "generic_name": "Gabapentin", "labeler_name": "American Health Packaging", "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": "20200302", "listing_expiration_date": "20261231"}