Claritin is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Bayer Healthcare Llc.. The primary component is Loratadine.
Product ID | 11523-7160_8242a0ef-e3e8-8e01-e053-2a91aa0abdc9 |
NDC | 11523-7160 |
Product Type | Human Otc Drug |
Proprietary Name | Claritin |
Generic Name | Loratadine |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 1993-04-12 |
Marketing Category | NDA / NDA |
Application Number | NDA019658 |
Labeler Name | Bayer HealthCare LLC. |
Substance Name | LORATADINE |
Active Ingredient Strength | 10 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 1993-04-12 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA019658 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1993-04-12 |
Marketing Category | NDA |
Application Number | NDA019658 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1993-04-12 |
Marketing Category | NDA |
Application Number | NDA019658 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1993-04-12 |
Marketing Category | NDA |
Application Number | NDA019658 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-09-01 |
Marketing Category | NDA |
Application Number | NDA019658 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 1993-04-12 |
Marketing Category | NDA |
Application Number | NDA019658 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 1993-04-12 |
Marketing Category | NDA |
Application Number | NDA019658 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 1993-04-12 |
Marketing Category | NDA |
Application Number | NDA019658 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 1993-04-12 |
Ingredient | Strength |
---|---|
LORATADINE | 10 mg/1 |
SPL SET ID: | 660ac9df-f1b1-4c89-94dd-9fae0a013f3c |
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RxNorm Concept Unique ID - RxCUI | |
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