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Dilaudid
Dilaudid - 55154-1610-1 - (hydromorphone hydrochloride)
Drug Information of Dilaudid
| Product NDC: | 55154-1610 |
| Proprietary Name: | Dilaudid |
| 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 Dilaudid
| Product NDC: | 55154-1610 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019892 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19260101 |
Package Information of Dilaudid
| Package NDC: | 55154-1610-1 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (55154-1610-1) |
NDC Information of Dilaudid
| NDC Code | 55154-1610-1 |
| Proprietary Name | Dilaudid |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (55154-1610-1) |
| Product NDC | 55154-1610 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydromorphone hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19260101 |
| Marketing Category Name | NDA |
| Labeler Name | Cardinal Health |
| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
