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ConRx Allergy
ConRx Allergy - 68737-230-14 - (Diphenhydramine Hydrochloride)
Drug Information of ConRx Allergy
| Product NDC: | 68737-230 |
| Proprietary Name: | ConRx Allergy |
| Non Proprietary Name: | Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ConRx Allergy
| Product NDC: | 68737-230 |
| Labeler Name: | Eagle Distributors,Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130215 |
Package Information of ConRx Allergy
| Package NDC: | 68737-230-14 |
| Package Description: | 50 POUCH in 1 BOX (68737-230-14) > 2 TABLET in 1 POUCH |
NDC Information of ConRx Allergy
| NDC Code | 68737-230-14 |
| Proprietary Name | ConRx Allergy |
| Package Description | 50 POUCH in 1 BOX (68737-230-14) > 2 TABLET in 1 POUCH |
| Product NDC | 68737-230 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130215 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Eagle Distributors,Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
