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DILAUDID
DILAUDID - 59011-452-10 - (HYDROMORPHONE HYDROCHLORIDE)
Drug Information of DILAUDID
| Product NDC: | 59011-452 |
| 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) |
Labeler Information of DILAUDID
| Product NDC: | 59011-452 |
| Labeler Name: | Purdue Pharma LP |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019892 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19260112 |
Package Information of DILAUDID
| Package NDC: | 59011-452-10 |
| Package Description: | 100 TABLET in 1 BOTTLE (59011-452-10) |
NDC Information of DILAUDID
| NDC Code | 59011-452-10 |
| Proprietary Name | DILAUDID |
| Package Description | 100 TABLET in 1 BOTTLE (59011-452-10) |
| Product NDC | 59011-452 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROMORPHONE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19260112 |
| Marketing Category Name | NDA |
| Labeler Name | Purdue Pharma LP |
| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
