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Hydromorphone Hydrochloride - 68084-472-01 - (Hydromorphone Hydrochloride)

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Drug Information of Hydromorphone Hydrochloride

Product NDC: 68084-472
Proprietary Name: Hydromorphone Hydrochloride
Non Proprietary Name: Hydromorphone Hydrochloride
Active Ingredient(s): 4    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: 68084-472
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078439
Marketing Category: ANDA
Start Marketing Date: 20110301

Package Information of Hydromorphone Hydrochloride

Package NDC: 68084-472-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-472-01) > 10 TABLET in 1 BLISTER PACK (68084-472-11)

NDC Information of Hydromorphone Hydrochloride

NDC Code 68084-472-01
Proprietary Name Hydromorphone Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (68084-472-01) > 10 TABLET in 1 BLISTER PACK (68084-472-11)
Product NDC 68084-472
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydromorphone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110301
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name HYDROMORPHONE HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Hydromorphone Hydrochloride


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