ORTHO-NOVUM 1 Drug Patent Profile
✉ Email this page to a colleague
Which patents cover Ortho-novum 1, and when can generic versions of Ortho-novum 1 launch?
Ortho-novum 1 is a drug marketed by Ortho Mcneil Pharm, Janssen Pharms, and Ortho Mcneil Janssen. and is included in six NDAs.
The generic ingredient in ORTHO-NOVUM 1 is mestranol; norethindrone. There are eleven drug master file entries for this compound. Additional details are available on the mestranol; norethindrone profile page.
AI Research Assistant
Questions you can ask:
- What is the 5 year forecast for ORTHO-NOVUM 1?
- What are the global sales for ORTHO-NOVUM 1?
- What is Average Wholesale Price for ORTHO-NOVUM 1?
Summary for ORTHO-NOVUM 1
US Patents: | 0 |
Applicants: | 3 |
NDAs: | 6 |
DailyMed Link: | ORTHO-NOVUM 1 at DailyMed |
US Patents and Regulatory Information for ORTHO-NOVUM 1
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Ortho Mcneil Pharm | ORTHO-NOVUM 1/35-21 | ethinyl estradiol; norethindrone | TABLET;ORAL-21 | 017489-002 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Ortho Mcneil Pharm | ORTHO-NOVUM 10-21 | mestranol; norethindrone | TABLET;ORAL-21 | 012728-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Ortho Mcneil Janssen | ORTHO-NOVUM 1/50 28 | mestranol; norethindrone | TABLET;ORAL-28 | 016709-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Ortho Mcneil Janssen | ORTHO-NOVUM 10/11-21 | ethinyl estradiol; norethindrone | TABLET;ORAL-21 | 018354-001 | Jan 11, 1982 | DISCN | Yes | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Janssen Pharms | ORTHO-NOVUM 1/35-28 | ethinyl estradiol; norethindrone | TABLET;ORAL-28 | 017919-002 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |