Details for New Drug Application (NDA): 204394
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The generic ingredient in MINOCYCLINE HYDROCHLORIDE is minocycline hydrochloride. There are fifteen drug master file entries for this compound. Twenty-six suppliers are listed for this compound. Additional details are available on the minocycline hydrochloride profile page.
Summary for 204394
| Tradename: | MINOCYCLINE HYDROCHLORIDE |
| Applicant: | Sun Pharm |
| Ingredient: | minocycline hydrochloride |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 204394
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 45MG BASE | ||||
| Approval Date: | Dec 30, 2015 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 55MG BASE | ||||
| Approval Date: | Oct 7, 2022 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 65MG BASE | ||||
| Approval Date: | Oct 7, 2022 | TE: | RLD: | No | |||||
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