gabapentin

Generic: gabapentin

Labeler: mckesson corporation dba sky packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler mckesson corporation dba sky packaging
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 300 mg/1

Manufacturer
McKesson Corporation dba Sky Packaging

Identifiers & Regulatory

Product NDC 63739-903
Product ID 63739-903_159496fe-700e-4c94-a766-7809a7ce1839
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090858
Listing Expiration 2026-12-31
Marketing Start 2021-07-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63739903
Hyphenated Format 63739-903

Supplemental Identifiers

RxCUI
310430 310431 310432
UPC
0363739902107
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 ANDA090858 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 CARTON (63739-903-10) / 10 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (1)

63739-903-10 10 BLISTER PACK in 1 CARTON (63739-903-10) / 10 CAPSULE in 1 BLISTER PACK

Ingredients (1)

gabapentin (300 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": "159496fe-700e-4c94-a766-7809a7ce1839", "openfda": {"nui": ["N0000008486"], "upc": ["0363739902107"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310431", "310432"], "spl_set_id": ["23eb133e-2f74-4219-9892-0a8e770ec032"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["McKesson Corporation dba Sky Packaging"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (63739-903-10)  / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "63739-903-10", "marketing_start_date": "20210715"}], "brand_name": "Gabapentin", "product_id": "63739-903_159496fe-700e-4c94-a766-7809a7ce1839", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "63739-903", "generic_name": "Gabapentin", "labeler_name": "McKesson Corporation dba Sky Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA090858", "marketing_category": "ANDA", "marketing_start_date": "20210715", "listing_expiration_date": "20261231"}