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HYDROMORPHONE HYDROCHLORIDE
HYDROMORPHONE HYDROCHLORIDE - 10544-374-56 - (HYDROMORPHONE HYDROCHLORIDE)
Drug Information of HYDROMORPHONE HYDROCHLORIDE
| Product NDC: | 10544-374 |
| Proprietary Name: | HYDROMORPHONE HYDROCHLORIDE |
| 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 HYDROMORPHONE HYDROCHLORIDE
| Product NDC: | 10544-374 |
| Labeler Name: | Blenheim Pharmacal, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078273 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080529 |
Package Information of HYDROMORPHONE HYDROCHLORIDE
| Package NDC: | 10544-374-56 |
| Package Description: | 56 TABLET in 1 BOTTLE (10544-374-56) |
NDC Information of HYDROMORPHONE HYDROCHLORIDE
| NDC Code | 10544-374-56 |
| Proprietary Name | HYDROMORPHONE HYDROCHLORIDE |
| Package Description | 56 TABLET in 1 BOTTLE (10544-374-56) |
| Product NDC | 10544-374 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROMORPHONE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080529 |
| Marketing Category Name | ANDA |
| Labeler Name | Blenheim Pharmacal, Inc. |
| Substance Name | HYDROMORPHONE HYDROCHLORIDE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
