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Levocetirizine Dihydrochloride
Levocetirizine Dihydrochloride - 0093-7701-98 - (Levocetirizine Dihydrochloride)
Drug Information of Levocetirizine Dihydrochloride
| Product NDC: | 0093-7701 |
| Proprietary Name: | Levocetirizine Dihydrochloride |
| Non Proprietary Name: | Levocetirizine Dihydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; Levocetirizine Dihydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levocetirizine Dihydrochloride
| Product NDC: | 0093-7701 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090199 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110906 |
Package Information of Levocetirizine Dihydrochloride
| Package NDC: | 0093-7701-98 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (0093-7701-98) |
NDC Information of Levocetirizine Dihydrochloride
| NDC Code | 0093-7701-98 |
| Proprietary Name | Levocetirizine Dihydrochloride |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (0093-7701-98) |
| Product NDC | 0093-7701 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levocetirizine Dihydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110906 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
