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Allergy Attack Relief to Go
Allergy Attack Relief to Go - 51596-009-01 - (DIPHENHYDRAMINE HYDROCHLORIDE)
Drug Information of Allergy Attack Relief to Go
| Product NDC: | 51596-009 |
| Proprietary Name: | Allergy Attack Relief to Go |
| Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 25 mg/1 & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allergy Attack Relief to Go
| Product NDC: | 51596-009 |
| Labeler Name: | Breakthrough Products Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121001 |
Package Information of Allergy Attack Relief to Go
| Package NDC: | 51596-009-01 |
| Package Description: | 1 POWDER in 1 POUCH (51596-009-01) |
NDC Information of Allergy Attack Relief to Go
| NDC Code | 51596-009-01 |
| Proprietary Name | Allergy Attack Relief to Go |
| Package Description | 1 POWDER in 1 POUCH (51596-009-01) |
| Product NDC | 51596-009 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20121001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Breakthrough Products Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
