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Hydromorphone Hydrochloride
Hydromorphone Hydrochloride - 54868-3165-6 - (Hydromorphone Hydrochloride)
Drug Information of Hydromorphone Hydrochloride
| Product NDC: | 54868-3165 |
| Proprietary Name: | Hydromorphone Hydrochloride |
| Non Proprietary Name: | Hydromorphone Hydrochloride |
| Active Ingredient(s): | 2 mg/1 & nbsp; Hydromorphone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydromorphone Hydrochloride
| Product NDC: | 54868-3165 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078273 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040920 |
Package Information of Hydromorphone Hydrochloride
| Package NDC: | 54868-3165-6 |
| Package Description: | 120 TABLET, FILM COATED in 1 BOTTLE (54868-3165-6) |
NDC Information of Hydromorphone Hydrochloride
| NDC Code | 54868-3165-6 |
| Proprietary Name | Hydromorphone Hydrochloride |
| Package Description | 120 TABLET, FILM COATED in 1 BOTTLE (54868-3165-6) |
| Product NDC | 54868-3165 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydromorphone Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20040920 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
