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ConZip - 68025-053-30 - (tramadol hydrochloride)
Drug Information of ConZip
| Product NDC: | 68025-053 |
| Proprietary Name: | ConZip |
| Non Proprietary Name: | tramadol hydrochloride |
| Active Ingredient(s): | 100 mg/1 & nbsp; tramadol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ConZip
| Product NDC: | 68025-053 |
| Labeler Name: | Vertical Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022370 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110831 |
Package Information of ConZip
| Package NDC: | 68025-053-30 |
| Package Description: | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68025-053-30) |
NDC Information of ConZip
| NDC Code | 68025-053-30 |
| Proprietary Name | ConZip |
| Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68025-053-30) |
| Product NDC | 68025-053 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tramadol hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110831 |
| Marketing Category Name | NDA |
| Labeler Name | Vertical Pharmaceuticals Inc. |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
