NDC 66715-9742

Claritin

Loratadine Tablet

Claritin is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Lil' Drug Store Products, Inc.. The primary component is Loratadine.

• Product ID: 66715-9742_f0e77162-c602-1a0f-e053-2a95a90ab714
• NDC: 66715-9742
• Product Type: Human Otc Drug
• Proprietary Name: Claritin
• Generic Name: Loratadine Tablet
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2022-06-01
• Marketing Category: ANDA /
• Application Number: ANDA075209
• Labeler Name: Lil' Drug Store Products, Inc.
• Substance Name: LORATADINE
• Active Ingredient Strength: 10 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 66715-9742-1

1 POUCH in 1 CARTON (66715-9742-1) > 1 TABLET in 1 POUCH

• Marketing Start Date: 2022-06-01
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Claritin" or generic name "Loratadine Tablet"

NDC	Brand Name	Generic Name
11523-0007	Claritin	loratadine
11523-0800	Claritin	loratadine
11523-1527	Claritin	Loratadine
11523-4328	Claritin	Loratadine
11523-4329	Claritin	Loratadine
11523-4330	Claritin	loratadine
11523-4331	Claritin	Loratadine
11523-4359	Claritin	Loratadine
11523-6655	Claritin	Loratadine
11523-7157	Claritin	Loratadine
11523-7160	Claritin	Loratadine
11523-7200	Claritin	Loratadine
11523-7202	Claritin	Loratadine
67751-153	Claritin	Claritin
11523-7237	Claritin	Claritin
73097-005	Claritin	Claritin
70518-2951	Claritin	Claritin