gabapentin

Generic: gabapentin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler proficient rx lp
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 300 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-532
Product ID 71205-532_3b668584-ca03-409b-b016-10c252899d4c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204989
Listing Expiration 2026-12-31
Marketing Start 2016-04-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205532
Hyphenated Format 71205-532

Supplemental Identifiers

RxCUI
310431
UPC
0371205532901
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 ANDA204989 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 14 CAPSULE in 1 BOTTLE (71205-532-14)
  • 15 CAPSULE in 1 BOTTLE (71205-532-15)
  • 30 CAPSULE in 1 BOTTLE (71205-532-30)
  • 60 CAPSULE in 1 BOTTLE (71205-532-60)
  • 120 CAPSULE in 1 BOTTLE (71205-532-72)
  • 90 CAPSULE in 1 BOTTLE (71205-532-90)
source: ndc

Packages (6)

71205-532-14 14 CAPSULE in 1 BOTTLE (71205-532-14) 71205-532-15 15 CAPSULE in 1 BOTTLE (71205-532-15) 71205-532-30 30 CAPSULE in 1 BOTTLE (71205-532-30) 71205-532-60 60 CAPSULE in 1 BOTTLE (71205-532-60) 71205-532-72 120 CAPSULE in 1 BOTTLE (71205-532-72) 71205-532-90 90 CAPSULE in 1 BOTTLE (71205-532-90)

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": "3b668584-ca03-409b-b016-10c252899d4c", "openfda": {"nui": ["N0000008486"], "upc": ["0371205532901"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["223a9216-6e07-49b9-8faf-bb4e529a6ae5"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE in 1 BOTTLE (71205-532-14)", "package_ndc": "71205-532-14", "marketing_start_date": "20220105"}, {"sample": false, "description": "15 CAPSULE in 1 BOTTLE (71205-532-15)", "package_ndc": "71205-532-15", "marketing_start_date": "20210204"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-532-30)", "package_ndc": "71205-532-30", "marketing_start_date": "20210204"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71205-532-60)", "package_ndc": "71205-532-60", "marketing_start_date": "20210204"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE (71205-532-72)", "package_ndc": "71205-532-72", "marketing_start_date": "20210525"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71205-532-90)", "package_ndc": "71205-532-90", "marketing_start_date": "20210204"}], "brand_name": "Gabapentin", "product_id": "71205-532_3b668584-ca03-409b-b016-10c252899d4c", "dosage_form": "CAPSULE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71205-532", "generic_name": "Gabapentin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA204989", "marketing_category": "ANDA", "marketing_start_date": "20160401", "listing_expiration_date": "20261231"}