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LoHist DM
LoHist DM - 68047-129-16 - (Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride)
Drug Information of LoHist DM
| Product NDC: | 68047-129 |
| Proprietary Name: | LoHist DM |
| Non Proprietary Name: | Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride |
| Active Ingredient(s): | 2; 10; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LoHist DM
| Product NDC: | 68047-129 |
| Labeler Name: | Larken Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120601 |
Package Information of LoHist DM
| Package NDC: | 68047-129-16 |
| Package Description: | 473 mL in 1 BOTTLE (68047-129-16) |
NDC Information of LoHist DM
| NDC Code | 68047-129-16 |
| Proprietary Name | LoHist DM |
| Package Description | 473 mL in 1 BOTTLE (68047-129-16) |
| Product NDC | 68047-129 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Larken Laboratories, Inc. |
| Substance Name | BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 2; 10; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
