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Hydromorphone Hydrochloride - 43063-051-06 - (Hydromorphone Hydrochloride)

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Drug Information of Hydromorphone Hydrochloride

Product NDC: 43063-051
Proprietary Name: Hydromorphone Hydrochloride
Non Proprietary Name: Hydromorphone Hydrochloride
Active Ingredient(s): 2    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: 43063-051
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078439
Marketing Category: ANDA
Start Marketing Date: 20091209

Package Information of Hydromorphone Hydrochloride

Package NDC: 43063-051-06
Package Description: 6 TABLET in 1 BOTTLE, PLASTIC (43063-051-06)

NDC Information of Hydromorphone Hydrochloride

NDC Code 43063-051-06
Proprietary Name Hydromorphone Hydrochloride
Package Description 6 TABLET in 1 BOTTLE, PLASTIC (43063-051-06)
Product NDC 43063-051
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 PD-Rx Pharmaceuticals, Inc.
Substance Name HYDROMORPHONE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Hydromorphone Hydrochloride


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