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Oxycodone HCl Controlled-Release
Oxycodone HCl Controlled-Release - 63304-400-01 - (Oxycodone HCl Controlled-Release)
Drug Information of Oxycodone HCl Controlled-Release
| Product NDC: | 63304-400 |
| Proprietary Name: | Oxycodone HCl Controlled-Release |
| Non Proprietary Name: | Oxycodone HCl Controlled-Release |
| Active Ingredient(s): | 10 mg/1 & nbsp; Oxycodone HCl Controlled-Release |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxycodone HCl Controlled-Release
| Product NDC: | 63304-400 |
| Labeler Name: | Ranbaxy Pharmaceuticals Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020553 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100201 |
Package Information of Oxycodone HCl Controlled-Release
| Package NDC: | 63304-400-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (63304-400-01) |
NDC Information of Oxycodone HCl Controlled-Release
| NDC Code | 63304-400-01 |
| Proprietary Name | Oxycodone HCl Controlled-Release |
| Package Description | 100 TABLET in 1 BOTTLE (63304-400-01) |
| Product NDC | 63304-400 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxycodone HCl Controlled-Release |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | NDA |
| Labeler Name | Ranbaxy Pharmaceuticals Inc |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
