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Allergy Relief
Allergy Relief - 37808-571-95 - (fexofenadine hydrochloride)
Drug Information of Allergy Relief
| Product NDC: | 37808-571 |
| Proprietary Name: | 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 Allergy Relief
| Product NDC: | 37808-571 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076447 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110622 |
Package Information of Allergy Relief
| Package NDC: | 37808-571-95 |
| Package Description: | 1 BOTTLE in 1 CARTON (37808-571-95) > 45 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of Allergy Relief
| NDC Code | 37808-571-95 |
| Proprietary Name | Allergy Relief |
| Package Description | 1 BOTTLE in 1 CARTON (37808-571-95) > 45 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 37808-571 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | fexofenadine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110622 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
