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ROBITUSSIN PEAK COLD MAXIMUM STRENGTH MULTI-SYMPTOM COLD
ROBITUSSIN PEAK COLD MAXIMUM STRENGTH MULTI-SYMPTOM COLD - 0031-8734-18 - (dextromethorphan HBr, guaifenesin, phenylephrine HCl)
Drug Information of ROBITUSSIN PEAK COLD MAXIMUM STRENGTH MULTI-SYMPTOM COLD
| Product NDC: | 0031-8734 |
| Proprietary Name: | ROBITUSSIN PEAK COLD MAXIMUM STRENGTH MULTI-SYMPTOM COLD |
| Non Proprietary Name: | dextromethorphan HBr, guaifenesin, phenylephrine HCl |
| Active Ingredient(s): | 10; 200; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; dextromethorphan HBr, guaifenesin, phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ROBITUSSIN PEAK COLD MAXIMUM STRENGTH MULTI-SYMPTOM COLD
| Product NDC: | 0031-8734 |
| Labeler Name: | Richmond Division of Wyeth |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110615 |
Package Information of ROBITUSSIN PEAK COLD MAXIMUM STRENGTH MULTI-SYMPTOM COLD
| Package NDC: | 0031-8734-18 |
| Package Description: | 1 BOTTLE in 1 CARTON (0031-8734-18) > 237 mL in 1 BOTTLE |
NDC Information of ROBITUSSIN PEAK COLD MAXIMUM STRENGTH MULTI-SYMPTOM COLD
| NDC Code | 0031-8734-18 |
| Proprietary Name | ROBITUSSIN PEAK COLD MAXIMUM STRENGTH MULTI-SYMPTOM COLD |
| Package Description | 1 BOTTLE in 1 CARTON (0031-8734-18) > 237 mL in 1 BOTTLE |
| Product NDC | 0031-8734 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan HBr, guaifenesin, phenylephrine HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110615 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Richmond Division of Wyeth |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10; 200; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
