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Zyrtec
Zyrtec - 50580-726-03 - (Cetirizine Hydrochloride)
Drug Information of Zyrtec
| Product NDC: | 50580-726 |
| Proprietary Name: | Zyrtec |
| Non Proprietary Name: | Cetirizine Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Cetirizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zyrtec
| Product NDC: | 50580-726 |
| Labeler Name: | McNeil Consumer Healthcare Division of McNeil-PPC, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA019835 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20081001 |
Package Information of Zyrtec
| Package NDC: | 50580-726-03 |
| Package Description: | 50 BLISTER PACK in 1 CARTON (50580-726-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Zyrtec
| NDC Code | 50580-726-03 |
| Proprietary Name | Zyrtec |
| Package Description | 50 BLISTER PACK in 1 CARTON (50580-726-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 50580-726 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20081001 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Healthcare Division of McNeil-PPC, Inc. |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
