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cetirizine hydrochloride
cetirizine hydrochloride - 29300-134-19 - (cetirizine hydrochloride)
Drug Information of cetirizine hydrochloride
| Product NDC: | 29300-134 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of cetirizine hydrochloride
| Product NDC: | 29300-134 |
| Labeler Name: | Unichem Pharmaceuticals (USA), Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078680 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101130 |
Package Information of cetirizine hydrochloride
| Package NDC: | 29300-134-19 |
| Package Description: | 1 BOTTLE in 1 CARTON (29300-134-19) > 90 TABLET in 1 BOTTLE |
NDC Information of cetirizine hydrochloride
| NDC Code | 29300-134-19 |
| Proprietary Name | cetirizine hydrochloride |
| Package Description | 1 BOTTLE in 1 CARTON (29300-134-19) > 90 TABLET in 1 BOTTLE |
| Product NDC | 29300-134 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | cetirizine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101130 |
| Marketing Category Name | ANDA |
| Labeler Name | Unichem Pharmaceuticals (USA), Inc. |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
