DURLAZA is a Oral Capsule, Extended Release in the Human Prescription Drug category. It is labeled and distributed by New Haven Pharmaceuticals, Inc.. The primary component is Aspirin.
Product ID | 58487-001_6461fd18-6b4d-809a-73f4-fd0c23a99291 |
NDC | 58487-001 |
Product Type | Human Prescription Drug |
Proprietary Name | DURLAZA |
Generic Name | Acetylsalicylic Acid |
Dosage Form | Capsule, Extended Release |
Route of Administration | ORAL |
Marketing Start Date | 2015-09-25 |
Marketing Category | NDA / NDA |
Application Number | NDA200671 |
Labeler Name | New Haven Pharmaceuticals, Inc. |
Substance Name | ASPIRIN |
Active Ingredient Strength | 163 mg/1 |
Pharm Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Platelet Aggregation Inhibitor [EPC],Decreased Platelet Aggregation [PE] |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2015-09-25 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA200671 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-09-25 |
Inactivation Date | 2020-01-31 |
Marketing Category | NDA |
Application Number | NDA200671 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-09-25 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
ASPIRIN | 162.5 mg/1 |
SPL SET ID: | 4c2a1403-3862-1efd-0a91-444989222b37 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
Pharm Class PE | |
PHarm Class EPC | |
NUI Code |
NDC | Brand Name | Generic Name |
---|---|---|
58487-001 | DURLAZA | Acetylsalicylic Acid |
73678-160 | Biovanta Double Action | Acetylsalicylic Acid |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DURLAZA 86041501 4851723 Live/Registered |
New Haven Pharmaceuticals, Inc. 2013-08-19 |