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ZUTRIPRO
ZUTRIPRO - 63717-876-99 - (hydrocodone bitartrate, chlorpheniramine maleate, and pseudoephedrine hydrochloride)
Drug Information of ZUTRIPRO
| Product NDC: | 63717-876 |
| Proprietary Name: | ZUTRIPRO |
| Non Proprietary Name: | hydrocodone bitartrate, chlorpheniramine maleate, and pseudoephedrine hydrochloride |
| Active Ingredient(s): | 4; 5; 60 mg/5mL; mg/5mL; mg/5mL & nbsp; hydrocodone bitartrate, chlorpheniramine maleate, and pseudoephedrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZUTRIPRO
| Product NDC: | 63717-876 |
| Labeler Name: | Hawthorn Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022439 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110608 |
Package Information of ZUTRIPRO
| Package NDC: | 63717-876-99 |
| Package Description: | 12 BOTTLE in 1 CARTON (63717-876-99) > 5 mL in 1 BOTTLE |
NDC Information of ZUTRIPRO
| NDC Code | 63717-876-99 |
| Proprietary Name | ZUTRIPRO |
| Package Description | 12 BOTTLE in 1 CARTON (63717-876-99) > 5 mL in 1 BOTTLE |
| Product NDC | 63717-876 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocodone bitartrate, chlorpheniramine maleate, and pseudoephedrine hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20110608 |
| Marketing Category Name | NDA |
| Labeler Name | Hawthorn Pharmaceuticals, Inc. |
| Substance Name | CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 4; 5; 60 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
