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 100 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-123
Product ID 72789-123_4af6aac1-9038-92a9-e063-6394a90ab0a1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090007
Listing Expiration 2027-12-31
Marketing Start 2015-12-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789123
Hyphenated Format 72789-123

Supplemental Identifiers

RxCUI
310430
UPC
0372789123905
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 ANDA090007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-123-30)
  • 60 CAPSULE in 1 BOTTLE, PLASTIC (72789-123-60)
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (72789-123-90)
source: ndc

Packages (3)

72789-123-30 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-123-30) 72789-123-60 60 CAPSULE in 1 BOTTLE, PLASTIC (72789-123-60) 72789-123-90 90 CAPSULE in 1 BOTTLE, PLASTIC (72789-123-90)

Ingredients (1)

gabapentin (100 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": "4af6aac1-9038-92a9-e063-6394a90ab0a1", "openfda": {"nui": ["N0000008486"], "upc": ["0372789123905"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["9814b76c-87c6-4746-b712-3269352a901b"], "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 (72789-123-30)", "package_ndc": "72789-123-30", "marketing_start_date": "20201019"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (72789-123-60)", "package_ndc": "72789-123-60", "marketing_start_date": "20201203"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (72789-123-90)", "package_ndc": "72789-123-90", "marketing_start_date": "20200925"}], "brand_name": "GABAPENTIN", "product_id": "72789-123_4af6aac1-9038-92a9-e063-6394a90ab0a1", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72789-123", "generic_name": "gabapentin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA090007", "marketing_category": "ANDA", "marketing_start_date": "20151230", "listing_expiration_date": "20271231"}