gabapentin

Generic: gabapentin

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler pd-rx pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

gabapentin 300 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-055
Product ID 72789-055_3ca9c072-d910-4e73-e063-6394a90a7223
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075350
Listing Expiration 2026-12-31
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 72789055
Hyphenated Format 72789-055

Supplemental Identifiers

RxCUI
310431
UPC
0372789055930
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 ANDA075350 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-30)
  • 45 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-45)
  • 60 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-60)
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-90)
  • 180 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-93)
source: ndc

Packages (5)

72789-055-30 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-30) 72789-055-45 45 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-45) 72789-055-60 60 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-60) 72789-055-90 90 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-90) 72789-055-93 180 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-93)

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": "3ca9c072-d910-4e73-e063-6394a90a7223", "openfda": {"nui": ["N0000008486"], "upc": ["0372789055930"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["b4c7388a-19d9-4e3a-83c9-4943fb855be4"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-30)", "package_ndc": "72789-055-30", "marketing_start_date": "20200224"}, {"sample": false, "description": "45 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-45)", "package_ndc": "72789-055-45", "marketing_start_date": "20200909"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-60)", "package_ndc": "72789-055-60", "marketing_start_date": "20200909"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-90)", "package_ndc": "72789-055-90", "marketing_start_date": "20200224"}, {"sample": false, "description": "180 CAPSULE in 1 BOTTLE, PLASTIC (72789-055-93)", "package_ndc": "72789-055-93", "marketing_start_date": "20200616"}], "brand_name": "Gabapentin", "product_id": "72789-055_3ca9c072-d910-4e73-e063-6394a90a7223", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72789-055", "generic_name": "Gabapentin", "labeler_name": "PD-Rx Pharmaceuticals, 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": "20261231"}