Gabapentin - 76237-164-30 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 76237-164
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 100    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 76237-164
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075350
Marketing Category: ANDA
Start Marketing Date: 20110829

Package Information of Gabapentin

Package NDC: 76237-164-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-164-30) > 5 CAPSULE in 1 BLISTER PACK

NDC Information of Gabapentin

NDC Code 76237-164-30
Proprietary Name Gabapentin
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-164-30) > 5 CAPSULE in 1 BLISTER PACK
Product NDC 76237-164
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110829
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name GABAPENTIN
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information