Product NDC: | 66007-212 |
Proprietary Name: | Childrens Allergy |
Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE |
Active Ingredient(s): | 12.5 mg/1 & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66007-212 |
Labeler Name: | Capricorn Pharma Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100929 |
Package NDC: | 66007-212-02 |
Package Description: | 3 BLISTER PACK in 1 CARTON (66007-212-02) > 6 TABLET in 1 BLISTER PACK (66007-212-01) |
NDC Code | 66007-212-02 |
Proprietary Name | Childrens Allergy |
Package Description | 3 BLISTER PACK in 1 CARTON (66007-212-02) > 6 TABLET in 1 BLISTER PACK (66007-212-01) |
Product NDC | 66007-212 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100929 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Capricorn Pharma Inc. |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 12.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes |