gabapentin

Generic: gabapentin

Labeler: creekwood pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name gabapentin
Generic Name gabapentin
Labeler creekwood pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

gabapentin 600 mg/1

Manufacturer
Creekwood Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 82619-145
Product ID 82619-145_26ce27e6-34a6-70d2-e063-6394a90a7c96
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205101
Listing Expiration 2026-12-31
Marketing Start 2024-09-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82619145
Hyphenated Format 82619-145

Supplemental Identifiers

RxCUI
310433 310434
UPC
0382619142020 0382619143034 0382619143027 0382619144017 0382619146011 0382619144024 0382619142013 0382619143010 0382619145014 0382619142037 0382619146028 0382619145021
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 ANDA205101 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (82619-145-01)
  • 500 TABLET in 1 BOTTLE (82619-145-02)
source: ndc

Packages (2)

82619-145-01 100 TABLET in 1 BOTTLE (82619-145-01) 82619-145-02 500 TABLET in 1 BOTTLE (82619-145-02)

Ingredients (1)

gabapentin (600 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": "26ce27e6-34a6-70d2-e063-6394a90a7c96", "openfda": {"nui": ["N0000008486"], "upc": ["0382619142020", "0382619143034", "0382619143027", "0382619144017", "0382619146011", "0382619144024", "0382619142013", "0382619143010", "0382619145014", "0382619142037", "0382619146028", "0382619145021"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["266ef369-0a56-f225-e063-6294a90a495e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Creekwood Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82619-145-01)", "package_ndc": "82619-145-01", "marketing_start_date": "20240901"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82619-145-02)", "package_ndc": "82619-145-02", "marketing_start_date": "20240901"}], "brand_name": "Gabapentin", "product_id": "82619-145_26ce27e6-34a6-70d2-e063-6394a90a7c96", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "82619-145", "generic_name": "Gabapentin", "labeler_name": "Creekwood Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20240901", "listing_expiration_date": "20261231"}