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Fentanyl buccal - 0591-3575-96 - (Fentanyl buccal)

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Drug Information of Fentanyl buccal

Product NDC: 0591-3575
Proprietary Name: Fentanyl buccal
Non Proprietary Name: Fentanyl buccal
Active Ingredient(s): 800    ug/1 & nbsp;   Fentanyl buccal
Administration Route(s): BUCCAL; ORAL; TRANSMUCOSAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl buccal

Product NDC: 0591-3575
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079075
Marketing Category: ANDA
Start Marketing Date: 20110107

Package Information of Fentanyl buccal

Package NDC: 0591-3575-96
Package Description: 7 BLISTER PACK in 1 CARTON (0591-3575-96) > 4 TABLET in 1 BLISTER PACK (0591-3575-04)

NDC Information of Fentanyl buccal

NDC Code 0591-3575-96
Proprietary Name Fentanyl buccal
Package Description 7 BLISTER PACK in 1 CARTON (0591-3575-96) > 4 TABLET in 1 BLISTER PACK (0591-3575-04)
Product NDC 0591-3575
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fentanyl buccal
Dosage Form Name TABLET
Route Name BUCCAL; ORAL; TRANSMUCOSAL
Start Marketing Date 20110107
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name FENTANYL CITRATE
Strength Number 800
Strength Unit ug/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl buccal


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