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Dallergy
Dallergy - 16477-160-01 - (CHLORCYCLIZINE HYDROCHLORIDE)
Drug Information of Dallergy
| Product NDC: | 16477-160 |
| Proprietary Name: | Dallergy |
| Non Proprietary Name: | CHLORCYCLIZINE HYDROCHLORIDE |
| Active Ingredient(s): | 25; 10 mg/1; mg/1 & nbsp; CHLORCYCLIZINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dallergy
| Product NDC: | 16477-160 |
| Labeler Name: | Laser Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111101 |
Package Information of Dallergy
| Package NDC: | 16477-160-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (16477-160-01) |
NDC Information of Dallergy
| NDC Code | 16477-160-01 |
| Proprietary Name | Dallergy |
| Package Description | 100 TABLET in 1 BOTTLE (16477-160-01) |
| Product NDC | 16477-160 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CHLORCYCLIZINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laser Pharmaceuticals, LLC |
| Substance Name | CHLORCYCLIZINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 25; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
