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TussiCaps
TussiCaps - 0095-0108-01 - (hydrocodone polistirex and chlorpheniramine polistirex)
Drug Information of TussiCaps
| Product NDC: | 0095-0108 |
| Proprietary Name: | TussiCaps |
| Non Proprietary Name: | hydrocodone polistirex and chlorpheniramine polistirex |
| Active Ingredient(s): | 8; 10 mg/1; mg/1 & nbsp; hydrocodone polistirex and chlorpheniramine polistirex |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TussiCaps
| Product NDC: | 0095-0108 |
| Labeler Name: | ECR Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077273 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110902 |
Package Information of TussiCaps
| Package NDC: | 0095-0108-01 |
| Package Description: | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0095-0108-01) |
NDC Information of TussiCaps
| NDC Code | 0095-0108-01 |
| Proprietary Name | TussiCaps |
| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0095-0108-01) |
| Product NDC | 0095-0108 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocodone polistirex and chlorpheniramine polistirex |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110902 |
| Marketing Category Name | ANDA |
| Labeler Name | ECR Pharmaceuticals |
| Substance Name | CHLORPHENIRAMINE; HYDROCODONE |
| Strength Number | 8; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
