LEADER Loratadine is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Cardinal Health. The primary component is Loratadine.
| Product ID | 37205-346_fe6bc6f0-dfff-49a9-8251-43dfa0a48df2 |
| NDC | 37205-346 |
| Product Type | Human Otc Drug |
| Proprietary Name | LEADER Loratadine |
| Generic Name | Loratadine |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2003-08-19 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076134 |
| Labeler Name | Cardinal Health |
| Substance Name | LORATADINE |
| Active Ingredient Strength | 10 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2003-08-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA076134 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2003-08-19 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076134 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-08-27 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076134 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2003-08-19 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076134 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2003-08-19 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076134 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-08-27 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076134 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-08-27 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| LORATADINE | 10 mg/1 |
| SPL SET ID: | e283afb8-9d26-4bd9-be77-e95e1d88aef8 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 37205-346 | LEADER Loratadine | LEADER Loratadine |
| 0363-1612 | allergy relief | Loratadine |
| 0113-7612 | Basic Care allergy relief | Loratadine |
| 0113-7500 | basic care childrens allergy relief | loratadine |
| 0113-7671 | Basic Care Childrens Allergy Relief | Loratadine |
| 0121-0849 | Childrens Loratadine | LORATADINE |
| 0363-2131 | Childrens Loratadine | Loratadine |
| 0363-4020 | CHILDRENS LORATADINE ODT | Loratadine |
| 0363-2092 | Childrens Wal-itin | Loratadine |
| 0363-2108 | Childrens Walitin | Loratadine |
| 0113-0612 | good sense allergy relief | Loratadine |
| 0113-1191 | good sense allergy relief | loratadine |
| 0113-1612 | good sense allergy relief | Loratadine |
| 0113-9755 | good sense allergy relief | loratadine |
| 0113-0671 | Good Sense childrens allergy relief | Loratadine |
| 0113-1019 | good sense childrens allergy relief | loratadine |
| 0113-1719 | good sense childrens allergy relief | Loratadine |
| 0363-0858 | Indoor Outdoor Allergy Relief | Loratadine |
| 0179-8317 | Loratadine | Loratadine |
| 0363-0522 | Loratadine | Loratadine |
| 0363-0527 | Loratadine | Loratadine |
| 0363-0752 | Loratadine | Loratadine |
| 0363-9603 | Loratadine | Loratadine |
| 0363-0699 | Wal itin | Loratadine |
| 0363-0754 | Wal-itin | LORATADINE |
| 0363-1686 | WAL-ITIN | LORATADINE |
| 0363-9150 | Wal-itin | Loratadine |
| 0363-2085 | Wal-itin Allergy Relief | Loratadine |