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EXALGO
EXALGO - 23635-432-01 - (Hydromorphone Hydrochloride)
Drug Information of EXALGO
| Product NDC: | 23635-432 |
| Proprietary Name: | EXALGO |
| Non Proprietary Name: | Hydromorphone Hydrochloride |
| Active Ingredient(s): | 32 mg/1 & nbsp; Hydromorphone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EXALGO
| Product NDC: | 23635-432 |
| Labeler Name: | Mallinckrodt, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021217 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120824 |
Package Information of EXALGO
| Package NDC: | 23635-432-01 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23635-432-01) |
NDC Information of EXALGO
| NDC Code | 23635-432-01 |
| Proprietary Name | EXALGO |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23635-432-01) |
| Product NDC | 23635-432 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydromorphone Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120824 |
| Marketing Category Name | NDA |
| Labeler Name | Mallinckrodt, Inc |
| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
| Strength Number | 32 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
