NDC 70332-105

Fanatrex

Gabapentin

Fanatrex is a Oral Kit in the Human Prescription Drug category. It is labeled and distributed by California Pharmaceuticals, Llc. The primary component is .

Product ID70332-105_28c7b43b-5ce4-60a0-e054-00144ff88e88
NDC70332-105
Product TypeHuman Prescription Drug
Proprietary NameFanatrex
Generic NameGabapentin
Dosage FormKit
Route of AdministrationORAL
Marketing Start Date2016-01-01
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameCalifornia Pharmaceuticals, LLC
Active Ingredient Strength0
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 70332-105-01

1 KIT in 1 KIT (70332-105-01) * 10.5 g in 1 BOTTLE, GLASS * 420 mL in 1 BOTTLE, PLASTIC
Marketing Start Date2016-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70332-105-01 [70332010501]

Fanatrex KIT
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-01-01
Inactivation Date2020-01-31

Drug Details

OpenFDA Data

SPL SET ID:2731faa1-a7a9-5c4d-e054-00144ff88e88
Manufacturer

NDC Crossover Matching brand name "Fanatrex" or generic name "Gabapentin"

NDCBrand NameGeneric Name
70332-105FanatrexFanatrex
43093-105FanatrexFanatrex
0093-4443GabapentinGabapentin
0093-4444GabapentinGabapentin
0143-3991GabapentinGabapentin
0143-3993GabapentinGabapentin
0143-3994GabapentinGabapentin
0143-9992GabapentinGabapentin
0143-9993GabapentinGabapentin
0143-9994GabapentinGabapentin
0071-0401Neurontingabapentin
0071-0513Neurontingabapentin
0071-0803Neurontingabapentin
0071-0805Neurontingabapentin
0071-0806Neurontingabapentin
0071-2012Neurontingabapentin
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