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CETIRIZINE HYDROCHLORIDE
CETIRIZINE HYDROCHLORIDE - 16714-271-02 - (CETIRIZINE HYDROCHLORIDE)
Drug Information of CETIRIZINE HYDROCHLORIDE
| Product NDC: | 16714-271 |
| Proprietary Name: | CETIRIZINE HYDROCHLORIDE |
| 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 CETIRIZINE HYDROCHLORIDE
| Product NDC: | 16714-271 |
| Labeler Name: | Northstar Rx LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078862 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091019 |
Package Information of CETIRIZINE HYDROCHLORIDE
| Package NDC: | 16714-271-02 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-271-02) |
NDC Information of CETIRIZINE HYDROCHLORIDE
| NDC Code | 16714-271-02 |
| Proprietary Name | CETIRIZINE HYDROCHLORIDE |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-271-02) |
| Product NDC | 16714-271 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CETIRIZINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091019 |
| Marketing Category Name | ANDA |
| Labeler Name | Northstar Rx LLC |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
