NDC 0781-5077-64 - 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
- 0781-5077
- Requested NDC
- 0781-5077-64
- Package NDCs from labels
- 0781-5077-01, 0781-5077-64
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2020-03-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drug Facts | REMEDYREPACK INC. | 2020-03-31 | HUMAN OTC DRUG LABEL |
| Loratadine - Bryant Ranch Prepack | Bryant Ranch Prepack | 2020-01-19 | HUMAN OTC DRUG LABEL |
| Loratadine - Bryant Ranch Prepack | Bryant Ranch Prepack | 2020-01-19 | HUMAN OTC DRUG LABEL |
| Loratadine - Sandoz Inc | Sandoz Inc | 2019-02-15 | HUMAN OTC DRUG LABEL |
| Loratadine - St. Mary’s Medical Park Pharmacy | St. Mary’s Medical Park Pharmacy | 2018-11-15 | HUMAN OTC DRUG LABEL |
| Loratadine - Contract Pharmacy Services-PA | Coupler Enterprises | Contract Pharmacy Services-PA | Coupler Enterprises | 2017-09-19 | HUMAN OTC DRUG LABEL |
| Drug Facts | NuCare Pharmaceuticals, Inc. | 2017-05-11 | HUMAN OTC DRUG LABEL |
| Loratadine - NCS HealthCare of KY, Inc dba Vangard Labs | NCS HealthCare of KY, Inc dba Vangard Labs | 2014-11-24 | HUMAN OTC DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0781-5077-01 | EA - Each | 0781-5077 | ee2bd65b-3fef-4be8-badd-bf30aea9e7c9 | 1 | 2012-07-24 |
| 0781-5077-64 | EA - Each | 0781-5077 | d1533bfe-0d09-41a8-b3de-70ebebf3c12b | 1 | 2012-07-24 |
| 0781-5077-76 | EA - Each | 0781-5077 | 7f0bca63-8292-4908-b293-10884106fc88 | 1 | 2013-02-11 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.