NDC 51672-2085-01 - Childrens Loratadine
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 51672-2085
- Requested NDC
- 51672-2085-01
- Package NDCs from labels
- 51672-2085-8, 51672-2085-4, 51672-2085-5, 51672-2085-1, 51672-2085-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd.
- Effective date
- 2026-07-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Children's Loratadine | Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd. | 2026-07-14 | HUMAN OTC DRUG LABEL |
| Childrens Loratadine - Aidarex Pharmaceuticals LLC | Aidarex Pharmaceuticals LLC | 2012-09-28 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-2085-1 | Childrens Loratadine | 1 in 1 CARTON | SOLUTION | 1 | 4 | |
| 51672-2085-1 | Childrens Loratadine | 240 mL in 1 BOTTLE | SOLUTION | 240 | 4 | |
| 51672-2085-4 | Childrens Loratadine | 1 in 1 CARTON | SOLUTION | 1 | 4 | |
| 51672-2085-4 | Childrens Loratadine | 60 mL in 1 BOTTLE | SOLUTION | 60 | 4 | |
| 51672-2085-5 | Childrens Loratadine | 180 mL in 1 BOTTLE | SOLUTION | 180 | 4 | |
| 51672-2085-5 | Childrens Loratadine | 1 in 1 CARTON | SOLUTION | 1 | 4 | |
| 51672-2085-8 | Childrens Loratadine | 120 mL in 1 BOTTLE | SOLUTION | 120 | 4 | |
| 51672-2085-8 | Childrens Loratadine | 1 in 1 CARTON | SOLUTION | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-2085 | CHILDRENS LORATADINE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] | 4 | Current NDC, Legacy NDC, 8 package rows | 20241222_12c8066a-3429-481e-b63a-7ea2b439a170.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-2085-8 | ML - Milliliter | 51672-2085 | 5184de2c-9fbe-4799-98ab-e9575e711178 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| Allergy | LORATADINE | Selder, S.A. de C.V. | afdb0117-dd2d-4ab1-a2f4-2a88b6bf5251 | 2016-12-22 | Warnings | 7AJO3BO7QN |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| Loratadine | LORATADINE | Mylan Pharmaceuticals Inc. | 3b307aea-5a68-4c82-959a-cda4ffbd0a4a | 2013-11-15 | Warnings | 7AJO3BO7QN |
| c378686f-8bf4-4fff-9b88-d5a18ce37135 | 2d8c4743-9a77-4ef5-81c8-a372312b9e65 | 2012-09-28 | Warnings | c378686f-8bf4-4fff-9b88-d5a18ce37135 2d8c4743-9a77-4ef5-81c8-a372312b9e65 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.