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Hydroxyzine Pamoate - 49999-701-00 - (Hydroxyzine Pamoate)

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Drug Information of Hydroxyzine Pamoate

Product NDC: 49999-701
Proprietary Name: Hydroxyzine Pamoate
Non Proprietary Name: Hydroxyzine Pamoate
Active Ingredient(s): 25    mg/1 & nbsp;   Hydroxyzine Pamoate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroxyzine Pamoate

Product NDC: 49999-701
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040156
Marketing Category: ANDA
Start Marketing Date: 19960715

Package Information of Hydroxyzine Pamoate

Package NDC: 49999-701-00
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (49999-701-00)

NDC Information of Hydroxyzine Pamoate

NDC Code 49999-701-00
Proprietary Name Hydroxyzine Pamoate
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (49999-701-00)
Product NDC 49999-701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Pamoate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19960715
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name HYDROXYZINE PAMOATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine Pamoate


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