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Fexofenadine hydrochloride
Fexofenadine hydrochloride - 55111-784-45 - (Fexofenadine hydrochloride)
Drug Information of Fexofenadine hydrochloride
| Product NDC: | 55111-784 |
| Proprietary Name: | Fexofenadine hydrochloride |
| Non Proprietary Name: | Fexofenadine hydrochloride |
| Active Ingredient(s): | 180 mg/1 & nbsp; Fexofenadine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fexofenadine hydrochloride
| Product NDC: | 55111-784 |
| Labeler Name: | Dr. Reddy's Laboratories Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076502 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110415 |
Package Information of Fexofenadine hydrochloride
| Package NDC: | 55111-784-45 |
| Package Description: | 45 TABLET in 1 BOTTLE (55111-784-45) |
NDC Information of Fexofenadine hydrochloride
| NDC Code | 55111-784-45 |
| Proprietary Name | Fexofenadine hydrochloride |
| Package Description | 45 TABLET in 1 BOTTLE (55111-784-45) |
| Product NDC | 55111-784 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Fexofenadine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110415 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr. Reddy's Laboratories Limited |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
