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biclora
biclora - 63717-332-06 - (Chlorphedianol Hydrochloride, Chlorcyclizine Hydrochloride)
Drug Information of biclora
| Product NDC: | 63717-332 |
| Proprietary Name: | biclora |
| Non Proprietary Name: | Chlorphedianol Hydrochloride, Chlorcyclizine Hydrochloride |
| Active Ingredient(s): | 25; 25 mg/1; mg/1 & nbsp; Chlorphedianol Hydrochloride, Chlorcyclizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of biclora
| Product NDC: | 63717-332 |
| Labeler Name: | Hawthorn Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121130 |
Package Information of biclora
| Package NDC: | 63717-332-06 |
| Package Description: | 60 TABLET in 1 BOTTLE (63717-332-06) |
NDC Information of biclora
| NDC Code | 63717-332-06 |
| Proprietary Name | biclora |
| Package Description | 60 TABLET in 1 BOTTLE (63717-332-06) |
| Product NDC | 63717-332 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlorphedianol Hydrochloride, Chlorcyclizine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121130 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Hawthorn Pharmaceuticals, Inc. |
| Substance Name | CHLOPHEDIANOL HYDROCHLORIDE; CHLORCYCLIZINE HYDROCHLORIDE |
| Strength Number | 25; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
