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fexofenadine hydrochloride
fexofenadine hydrochloride - 49349-890-20 - (fexofenadine hydrochloride)
Drug Information of fexofenadine hydrochloride
| Product NDC: | 49349-890 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of fexofenadine hydrochloride
| Product NDC: | 49349-890 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076447 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130520 |
Package Information of fexofenadine hydrochloride
| Package NDC: | 49349-890-20 |
| Package Description: | 100 TABLET, FILM COATED in 1 VIAL (49349-890-20) |
NDC Information of fexofenadine hydrochloride
| NDC Code | 49349-890-20 |
| Proprietary Name | fexofenadine hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 VIAL (49349-890-20) |
| Product NDC | 49349-890 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fexofenadine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130520 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
