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Antihistimine Allergy
Antihistimine Allergy - 59726-690-01 - (DIPHENHYDRAMINE HYDROCHLORIDE)
Drug Information of Antihistimine Allergy
| Product NDC: | 59726-690 |
| Proprietary Name: | Antihistimine 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 Antihistimine Allergy
| Product NDC: | 59726-690 |
| Labeler Name: | P and L Development of New York Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111208 |
Package Information of Antihistimine Allergy
| Package NDC: | 59726-690-01 |
| Package Description: | 1 BOTTLE in 1 BOX (59726-690-01) > 100 TABLET in 1 BOTTLE |
NDC Information of Antihistimine Allergy
| NDC Code | 59726-690-01 |
| Proprietary Name | Antihistimine Allergy |
| Package Description | 1 BOTTLE in 1 BOX (59726-690-01) > 100 TABLET in 1 BOTTLE |
| Product NDC | 59726-690 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111208 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | P and L Development of New York Company |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
