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Minocycline hydrochloride

Minocycline HCL 100mg Capsules

Approved
Approval ID

f901a1ba-1716-8795-e053-6294a90a4e77

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Apr 10, 2023

Manufacturers
FDA

Advanced Rx Pharmacy of Tennessee, LLC

DUNS: 117023142

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Minocycline hydrochloride

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code80425-0314
Application NumberANDA065062
Product Classification
M
Marketing Category
C73584
G
Generic Name
Minocycline hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateApril 10, 2023
FDA Product Classification

INGREDIENTS (1)

MINOCYCLINE HYDROCHLORIDEActive
Quantity: 100 mg in 1 1
Code: 0020414E5U
Classification: ACTIM

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Minocycline hydrochloride - FDA Drug Approval Details