SUBVENITE is a Kit in the Human Prescription Drug category. It is labeled and distributed by Owp Pharmaceuticals, Inc.. The primary component is .
Product ID | 69102-306_87a84064-9191-4025-bafe-297a6dd86407 |
NDC | 69102-306 |
Product Type | Human Prescription Drug |
Proprietary Name | SUBVENITE |
Generic Name | Lamotrigine |
Dosage Form | Kit |
Marketing Start Date | 2018-04-14 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA078947 |
Labeler Name | OWP Pharmaceuticals, Inc. |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2018-04-14 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA078947 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2018-04-14 |
SPL SET ID: | 7ad18b68-ba16-4810-9c3e-27fa970454e8 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
69102-306 | SUBVENITE | SUBVENITE |
69102-301 | SUBVENITE | SUBVENITE |
69102-312 | SUBVENITE | SUBVENITE |
69102-300 | SUBVENITE | SUBVENITE |
69102-150 | SUBVENITE | SUBVENITE |
69102-319 | SUBVENITE | SUBVENITE |
69102-320 | SUBVENITE | SUBVENITE |
70518-2645 | SUBVENITE | SUBVENITE |
0093-0039 | Lamotrigine | Lamotrigine |
0093-0132 | Lamotrigine | Lamotrigine |
0093-0463 | Lamotrigine | Lamotrigine |
0093-0688 | Lamotrigine | Lamotrigine |
0093-7247 | Lamotrigine | Lamotrigine |
0093-7248 | Lamotrigine | Lamotrigine |
0115-1526 | Lamotrigine | LAMOTRIGINE |
0115-1527 | Lamotrigine | LAMOTRIGINE |
0115-1528 | Lamotrigine | LAMOTRIGINE |
0115-1529 | Lamotrigine | LAMOTRIGINE |
0115-9939 | Lamotrigine | LAMOTRIGINE |
0115-9940 | Lamotrigine | LAMOTRIGINE |
0115-9941 | Lamotrigine | LAMOTRIGINE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SUBVENITE 87690016 not registered Live/Pending |
OWP Pharmaceuticals, Inc. 2017-11-17 |