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Hydromorphone Hydrochloride - 52959-413-02 - (Hydromorphone Hydrochloride)

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Drug Information of Hydromorphone Hydrochloride

Product NDC: 52959-413
Proprietary Name: Hydromorphone Hydrochloride
Non Proprietary Name: Hydromorphone Hydrochloride
Active Ingredient(s): 8    mg/1 & nbsp;   Hydromorphone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydromorphone Hydrochloride

Product NDC: 52959-413
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077471
Marketing Category: ANDA
Start Marketing Date: 20091209

Package Information of Hydromorphone Hydrochloride

Package NDC: 52959-413-02
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (52959-413-02)

NDC Information of Hydromorphone Hydrochloride

NDC Code 52959-413-02
Proprietary Name Hydromorphone Hydrochloride
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (52959-413-02)
Product NDC 52959-413
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydromorphone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091209
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name HYDROMORPHONE HYDROCHLORIDE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Hydromorphone Hydrochloride


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