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Indoor/Outdoor ALLERGY RELIEF Softgels
Indoor/Outdoor ALLERGY RELIEF Softgels - 59779-415-30 - (Cetirizine Hydrochloride)
Drug Information of Indoor/Outdoor ALLERGY RELIEF Softgels
| Product NDC: | 59779-415 |
| Proprietary Name: | Indoor/Outdoor ALLERGY RELIEF Softgels |
| Non Proprietary Name: | Cetirizine Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Cetirizine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Indoor/Outdoor ALLERGY RELIEF Softgels
| Product NDC: | 59779-415 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA022429 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130301 |
Package Information of Indoor/Outdoor ALLERGY RELIEF Softgels
| Package NDC: | 59779-415-30 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 PACKAGE (59779-415-30) > 30 CAPSULE in 1 BOTTLE, PLASTIC |
NDC Information of Indoor/Outdoor ALLERGY RELIEF Softgels
| NDC Code | 59779-415-30 |
| Proprietary Name | Indoor/Outdoor ALLERGY RELIEF Softgels |
| Package Description | 1 BOTTLE, PLASTIC in 1 PACKAGE (59779-415-30) > 30 CAPSULE in 1 BOTTLE, PLASTIC |
| Product NDC | 59779-415 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130301 |
| Marketing Category Name | NDA |
| Labeler Name | CVS Pharmacy |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
