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Fexofenadine Hydrochloride
Fexofenadine Hydrochloride - 49999-772-30 - (Fexofenadine Hydrochloride)
Drug Information of Fexofenadine Hydrochloride
| Product NDC: | 49999-772 |
| 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: | 49999-772 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA020872 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100607 |
Package Information of Fexofenadine Hydrochloride
| Package NDC: | 49999-772-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-772-30) |
NDC Information of Fexofenadine Hydrochloride
| NDC Code | 49999-772-30 |
| Proprietary Name | Fexofenadine Hydrochloride |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-772-30) |
| Product NDC | 49999-772 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fexofenadine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100607 |
| Marketing Category Name | ANDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
