gabapentin

Generic: gabapentin

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler actavis pharma, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 300 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 45963-556
Product ID 45963-556_3eb9a703-1a91-40a0-ab50-d42cefb454fa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075350
Listing Expiration 2027-12-31
Marketing Start 2014-04-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 45963556
Hyphenated Format 45963-556

Supplemental Identifiers

RxCUI
310430 310431 310432
UPC
0345963555113 0345963556110
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 ANDA075350 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (45963-556-11)
  • 500 CAPSULE in 1 BOTTLE (45963-556-50)
source: ndc

Packages (2)

Ingredients (1)

gabapentin (300 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3eb9a703-1a91-40a0-ab50-d42cefb454fa", "openfda": {"nui": ["N0000008486"], "upc": ["0345963555113", "0345963556110"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310431", "310432"], "spl_set_id": ["5969871e-6c71-4c37-9d63-370718ccc80c"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (45963-556-11)", "package_ndc": "45963-556-11", "marketing_start_date": "20140403"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (45963-556-50)", "package_ndc": "45963-556-50", "marketing_end_date": "20280531", "marketing_start_date": "20140512"}], "brand_name": "Gabapentin", "product_id": "45963-556_3eb9a703-1a91-40a0-ab50-d42cefb454fa", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "45963-556", "generic_name": "Gabapentin", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA075350", "marketing_category": "ANDA", "marketing_start_date": "20140403", "listing_expiration_date": "20271231"}