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up and up allergy relief
up and up allergy relief - 11673-571-22 - (fexofenadine hydrochloride)
Drug Information of up and up allergy relief
| Product NDC: | 11673-571 |
| Proprietary Name: | up and up allergy relief |
| Non Proprietary Name: | fexofenadine hydrochloride |
| Active Ingredient(s): | 180 mg/1 & nbsp; fexofenadine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of up and up allergy relief
| Product NDC: | 11673-571 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076447 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110413 |
Package Information of up and up allergy relief
| Package NDC: | 11673-571-22 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (11673-571-22) > 5 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of up and up allergy relief
| NDC Code | 11673-571-22 |
| Proprietary Name | up and up allergy relief |
| Package Description | 3 BLISTER PACK in 1 CARTON (11673-571-22) > 5 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 11673-571 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | fexofenadine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110413 |
| Marketing Category Name | ANDA |
| Labeler Name | Target Corporation |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
