SUNMARK 12 HOUR ALLERGY RELIEF is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Mckesson. The primary component is Clemastine Fumarate.
| Product ID | 49348-686_8d6e2187-3eb1-4b3d-b6f3-539816ccdcd2 |
| NDC | 49348-686 |
| Product Type | Human Otc Drug |
| Proprietary Name | SUNMARK 12 HOUR ALLERGY RELIEF |
| Generic Name | Clemastine Fumarate |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2003-07-03 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA074512 |
| Labeler Name | McKesson |
| Substance Name | CLEMASTINE FUMARATE |
| Active Ingredient Strength | 1 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2003-07-03 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA074512 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2003-07-03 |
| Ingredient | Strength |
|---|---|
| CLEMASTINE FUMARATE | 1.34 mg/1 |
| SPL SET ID: | 539e2c02-b258-45ea-8694-58ce5165ea7c |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 49348-686 | SUNMARK 12 HOUR ALLERGY RELIEF | Clemastine fumarate |
| 0093-0308 | Clemastine Fumarate | Clemastine Fumarate |
| 51655-425 | Clemastine Fumarate | Clemastine Fumarate |
| 54838-514 | Clemastine Fumarate | Clemastine Fumarate |
| 68151-2456 | Clemastine Fumarate | Clemastine Fumarate |
| 73308-358 | Clemastine Fumarate | Clemastine Fumarate |
| 42507-282 | Dayhist allergy | Clemastine fumarate |
| 24385-183 | Good Neighbor Pharmacy Dayhist Allergy | Clemastine fumarate |
| 70000-0216 | Leader Allerhist | Clemastine fumarate |
| 0363-0707 | wal hist | Clemastine fumarate |