Details for New Drug Application (NDA): 012772
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The generic ingredient in HALDRONE is paramethasone acetate. There are two drug master file entries for this compound. Additional details are available on the paramethasone acetate profile page.
Summary for 012772
| Tradename: | HALDRONE |
| Applicant: | Lilly |
| Ingredient: | paramethasone acetate |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 012772
Profile for product number 005
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 1MG | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | No | |||||
Profile for product number 006
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 2MG | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | No | |||||
Expired US Patents for NDA 012772
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
|---|---|---|---|---|---|---|---|
| Lilly | HALDRONE | paramethasone acetate | TABLET;ORAL | 012772-005 | Approved Prior to Jan 1, 1982 | 3,499,016 | ⤷ Start Trial |
| Lilly | HALDRONE | paramethasone acetate | TABLET;ORAL | 012772-006 | Approved Prior to Jan 1, 1982 | 3,499,016 | ⤷ Start Trial |
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
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