AUROVELA Drug Patent Profile
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When do Aurovela patents expire, and when can generic versions of Aurovela launch?
Aurovela is a drug marketed by Aurobindo Pharma and is included in five NDAs.
The generic ingredient in AUROVELA is ethinyl estradiol; norethindrone acetate. There are twenty-six drug master file entries for this compound. Twenty-five suppliers are listed for this compound. Additional details are available on the ethinyl estradiol; norethindrone acetate profile page.
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Questions you can ask:
- What is the 5 year forecast for AUROVELA?
- What are the global sales for AUROVELA?
- What is Average Wholesale Price for AUROVELA?
Summary for AUROVELA
| US Patents: | 0 |
| Applicants: | 1 |
| NDAs: | 5 |
| Drug Prices: | Drug price information for AUROVELA |
| DailyMed Link: | AUROVELA at DailyMed |
US Patents and Regulatory Information for AUROVELA
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Aurobindo Pharma | AUROVELA 1.5/30 | ethinyl estradiol; norethindrone acetate | TABLET;ORAL-21 | 207581-001 | Jun 26, 2017 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Aurobindo Pharma | AUROVELA FE 1.5/30 | ethinyl estradiol; norethindrone acetate | TABLET;ORAL-28 | 207580-001 | Jun 15, 2017 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Aurobindo Pharma | AUROVELA 1/20 | ethinyl estradiol; norethindrone acetate | TABLET;ORAL-21 | 207506-001 | Jun 16, 2017 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Aurobindo Pharma | AUROVELA 24 FE | ethinyl estradiol; norethindrone acetate | TABLET;ORAL | 207504-001 | Jun 15, 2017 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
