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Levocetirizine dihydrochloride
Levocetirizine dihydrochloride - 63672-0051-0 - (Levocetirizine dihydrochloride)
Drug Information of Levocetirizine dihydrochloride
| Product NDC: | 63672-0051 |
| 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: | 63672-0051 |
| Labeler Name: | Synthon Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090229 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101126 |
Package Information of Levocetirizine dihydrochloride
| Package NDC: | 63672-0051-0 |
| Package Description: | 87000 TABLET, FILM COATED in 1 DRUM (63672-0051-0) |
NDC Information of Levocetirizine dihydrochloride
| NDC Code | 63672-0051-0 |
| Proprietary Name | Levocetirizine dihydrochloride |
| Package Description | 87000 TABLET, FILM COATED in 1 DRUM (63672-0051-0) |
| Product NDC | 63672-0051 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levocetirizine dihydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101126 |
| Marketing Category Name | ANDA |
| Labeler Name | Synthon Pharmaceuticals, Inc. |
| Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
