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Hydromorphone Hydrochloride - 0641-2341-41 - (Hydromorphone Hydrochloride)

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Drug Information of Hydromorphone Hydrochloride

Product NDC: 0641-2341
Proprietary Name: Hydromorphone Hydrochloride
Non Proprietary Name: Hydromorphone Hydrochloride
Active Ingredient(s): 2    mg/mL & nbsp;   Hydromorphone Hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hydromorphone Hydrochloride

Product NDC: 0641-2341
Labeler Name: West-ward Pharmaceutical Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19720101

Package Information of Hydromorphone Hydrochloride

Package NDC: 0641-2341-41
Package Description: 20 VIAL in 1 CARTON (0641-2341-41) > 20 mL in 1 VIAL (0641-2341-39)

NDC Information of Hydromorphone Hydrochloride

NDC Code 0641-2341-41
Proprietary Name Hydromorphone Hydrochloride
Package Description 20 VIAL in 1 CARTON (0641-2341-41) > 20 mL in 1 VIAL (0641-2341-39)
Product NDC 0641-2341
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydromorphone Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19720101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name West-ward Pharmaceutical Corp.
Substance Name HYDROMORPHONE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Hydromorphone Hydrochloride


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