Amethia is a Kit in the Human Prescription Drug category. It is labeled and distributed by Mayne Pharma Inc. The primary component is .
Product ID | 51862-047_3c0c7e77-ed9d-46a7-8052-501e6e565fe9 |
NDC | 51862-047 |
Product Type | Human Prescription Drug |
Proprietary Name | Amethia |
Generic Name | Ethinyl Estradiol And Levonorgestrel |
Dosage Form | Kit |
Marketing Start Date | 2016-10-12 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA078834 |
Labeler Name | Mayne Pharma Inc |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2016-10-12 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA078834 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-10-12 |
Marketing Category | ANDA |
Application Number | ANDA078834 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-10-12 |
SPL SET ID: | d6a33ea7-ecd1-4f81-a984-f210a3989618 |
Manufacturer | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
51862-047 | Amethia | ETHINYL ESTRADIOL and LEVONORGESTREL |
0378-6550 | LEVONORGESTREL AND ETHINYL ESTRADIOL | ethinyl estradiol and levonorgestrel |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AMETHIA 90165336 not registered Live/Pending |
Mayne Pharma LLC 2020-09-08 |
AMETHIA 85048077 4032436 Dead/Cancelled |
MAYNE PHARMA LLC 2010-05-26 |
AMETHIA 78893196 not registered Dead/Abandoned |
Watson Pharmaceuticals, Inc. 2006-05-25 |