Details for New Drug Application (NDA): 090867
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The generic ingredient in MINOCYCLINE HYDROCHLORIDE is minocycline hydrochloride. There are fifteen drug master file entries for this compound. Thirty-five suppliers are listed for this compound. Additional details are available on the minocycline hydrochloride profile page.
Summary for 090867
Tradename: | MINOCYCLINE HYDROCHLORIDE |
Applicant: | Sun Pharm Inds Inc |
Ingredient: | minocycline hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 090867
Physiological Effect | Decreased Prothrombin Activity |
Medical Subject Heading (MeSH) Categories for 090867
Suppliers and Packaging for NDA: 090867
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
MINOCYCLINE HYDROCHLORIDE | minocycline hydrochloride | CAPSULE;ORAL | 090867 | ANDA | A-S Medication Solutions | 50090-5710 | 50090-5710-0 | 60 CAPSULE in 1 BOTTLE (50090-5710-0) |
MINOCYCLINE HYDROCHLORIDE | minocycline hydrochloride | CAPSULE;ORAL | 090867 | ANDA | A-S Medication Solutions | 50090-5710 | 50090-5710-3 | 90 CAPSULE in 1 BOTTLE (50090-5710-3) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 50MG BASE | ||||
Approval Date: | May 13, 2013 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 75MG BASE | ||||
Approval Date: | May 13, 2013 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 100MG BASE | ||||
Approval Date: | May 13, 2013 | TE: | AB | RLD: | No |
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