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Tussionex Pennkinetic
Tussionex Pennkinetic - 53014-548-01 - (hydrocodone polistirex and chlorpheniramine polistirex)
Drug Information of Tussionex Pennkinetic
| Product NDC: | 53014-548 |
| Proprietary Name: | Tussionex Pennkinetic |
| Non Proprietary Name: | hydrocodone polistirex and chlorpheniramine polistirex |
| Active Ingredient(s): | 8; 10 mg/5mL; mg/5mL & nbsp; hydrocodone polistirex and chlorpheniramine polistirex |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tussionex Pennkinetic
| Product NDC: | 53014-548 |
| Labeler Name: | UCB Manufacturing Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019111 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19871231 |
Package Information of Tussionex Pennkinetic
| Package NDC: | 53014-548-01 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (53014-548-01) > 115 mL in 1 BOTTLE, GLASS |
NDC Information of Tussionex Pennkinetic
| NDC Code | 53014-548-01 |
| Proprietary Name | Tussionex Pennkinetic |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (53014-548-01) > 115 mL in 1 BOTTLE, GLASS |
| Product NDC | 53014-548 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocodone polistirex and chlorpheniramine polistirex |
| Dosage Form Name | SUSPENSION, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19871231 |
| Marketing Category Name | NDA |
| Labeler Name | UCB Manufacturing Inc |
| Substance Name | CHLORPHENIRAMINE; HYDROCODONE |
| Strength Number | 8; 10 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Opioid Agonist [EPC],Opioid Agonists [MoA] |
