Product NDC: | 35356-514 |
Proprietary Name: | Dilaudid |
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) |
Product NDC: | 35356-514 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019892 |
Marketing Category: | NDA |
Start Marketing Date: | 20111201 |
Package NDC: | 35356-514-30 |
Package Description: | 30 TABLET in 1 BOTTLE (35356-514-30) |
NDC Code | 35356-514-30 |
Proprietary Name | Dilaudid |
Package Description | 30 TABLET in 1 BOTTLE (35356-514-30) |
Product NDC | 35356-514 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | hydromorphone hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20111201 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | HYDROMORPHONE HYDROCHLORIDE |
Strength Number | 2 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |