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 TABLET, FILM COATED
Routes
ORAL
Active Ingredients

gabapentin 800 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-160
Product ID 71205-160_982c815d-046b-47a5-abf7-f8a0c836543e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203244
Listing Expiration 2026-12-31
Marketing Start 2014-01-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205160
Hyphenated Format 71205-160

Supplemental Identifiers

RxCUI
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 ANDA203244 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-160-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-160-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-160-90)
source: ndc

Packages (3)

71205-160-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-160-30) 71205-160-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-160-60) 71205-160-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-160-90)

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": "982c815d-046b-47a5-abf7-f8a0c836543e", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["c09c66fd-cb31-41dd-b00b-acc58bd809f7"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-160-30)", "package_ndc": "71205-160-30", "marketing_start_date": "20181101"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-160-60)", "package_ndc": "71205-160-60", "marketing_start_date": "20181101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-160-90)", "package_ndc": "71205-160-90", "marketing_start_date": "20181101"}], "brand_name": "Gabapentin", "product_id": "71205-160_982c815d-046b-47a5-abf7-f8a0c836543e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71205-160", "generic_name": "GABAPENTIN", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA203244", "marketing_category": "ANDA", "marketing_start_date": "20140111", "listing_expiration_date": "20261231"}