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 |