Loratadine and Pseudoephedrine is a Oral Tablet, Extended Release in the Human Otc Drug category. It is labeled and distributed by Ohm Laboratories Inc.. The primary component is Loratadine; Pseudoephedrine Sulfate.
| Product ID | 51660-724_17d4b57e-a809-46ff-a15c-b5550a37a1c1 |
| NDC | 51660-724 |
| Product Type | Human Otc Drug |
| Proprietary Name | Loratadine and Pseudoephedrine |
| Generic Name | Loratadine And Pseudoephedrine |
| Dosage Form | Tablet, Extended Release |
| Route of Administration | ORAL |
| Marketing Start Date | 2004-11-17 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076557 |
| Labeler Name | Ohm Laboratories Inc. |
| Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
| Active Ingredient Strength | 10 mg/1; mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2004-11-17 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA076557 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-11-17 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076557 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-11-17 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076557 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-11-17 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076557 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2004-11-17 |
| Marketing End Date | 2013-04-19 |
| Marketing Category | ANDA |
| Application Number | ANDA076557 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2004-11-17 |
| Marketing End Date | 2013-04-19 |
| Marketing Category | ANDA |
| Application Number | ANDA076557 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2004-11-17 |
| Marketing End Date | 2013-04-19 |
| Ingredient | Strength |
|---|---|
| LORATADINE | 10 mg/1 |
| SPL SET ID: | 556b89ef-3b51-4faa-afb4-767a5c1b6422 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0363-0725 | Loratadine and Pseudoephedrine | Loratadine and Pseudoephedrine |
| 11822-9990 | Loratadine and Pseudoephedrine | LORATADINE and PSEUDOEPHEDRINE SULFATE |
| 21695-729 | Loratadine and Pseudoephedrine | loratadine and pseudoephedrine |
| 41163-165 | Loratadine and Pseudoephedrine | Loratadine and Pseudoephedrine |
| 46122-383 | Loratadine and Pseudoephedrine | loratadine and pseudoephedrine |
| 51660-488 | Loratadine and Pseudoephedrine | loratadine and pseudoephedrine |
| 51660-491 | Loratadine and Pseudoephedrine | loratadine and pseudoephedrine |
| 51660-724 | Loratadine and Pseudoephedrine | loratadine and pseudoephedrine |
| 61715-016 | Loratadine and Pseudoephedrine | Loratadine and Pseudoephedrine |
| 63187-305 | Loratadine and Pseudoephedrine | loratadine and pseudoephedrine |
| 63629-7766 | Loratadine and Pseudoephedrine | loratadine and pseudoephedrine |
| 70518-0653 | Loratadine and Pseudoephedrine | loratadine and pseudoephedrine |
| 59779-726 | ALLERGY RELIEF-D | Loratadine and Pseudoephedrine |