Claritin is a Oral Tablet, Chewable in the Human Otc Drug category. It is labeled and distributed by Bayer Healthcare Llc.. The primary component is Loratadine.
Product ID | 11523-4328_823163e2-b273-431d-e053-2991aa0a9ae8 |
NDC | 11523-4328 |
Product Type | Human Otc Drug |
Proprietary Name | Claritin |
Generic Name | Loratadine |
Dosage Form | Tablet, Chewable |
Route of Administration | ORAL |
Marketing Start Date | 2006-08-23 |
Marketing Category | NDA / NDA |
Application Number | NDA021891 |
Labeler Name | Bayer HealthCare LLC. |
Substance Name | LORATADINE |
Active Ingredient Strength | 5 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2006-08-23 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA021891 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-08-23 |
Marketing Category | NDA |
Application Number | NDA021891 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2006-08-23 |
Marketing Category | NDA |
Application Number | NDA021891 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-08-23 |
Marketing Category | NDA |
Application Number | NDA021891 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2006-08-23 |
Marketing Category | NDA |
Application Number | NDA021891 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-08-23 |
Marketing Category | NDA |
Application Number | NDA021891 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-08-23 |
Marketing Category | NDA |
Application Number | NDA021891 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2006-08-23 |
Marketing Category | NDA |
Application Number | NDA021891 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2006-08-23 |
Ingredient | Strength |
---|---|
LORATADINE | 5 mg/1 |
SPL SET ID: | 37732ca2-b454-4215-91a2-c62e0f7a56af |
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