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NDC 64380-0156-01

Minocycline Hydrochloride 100 mg/1 TABLET

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NDC
64380-0156-01
Generic Name
Minocycline Hydrochloride
Brand Name
Minocycline Hydrochloride
Strength
100 mg/1
Dosage Form
TABLET
Route
ORAL
Package Size
—
Labeler
Strides Pharma Science Limited

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Minocycline hydrochloride tablets are indicated in the treatment of the following infections due to susceptible strains of the designated microorganisms: Rocky Mountain spotted fever, typhus fever and the typhus group, Q fever, rickettsialpox and tick fevers caused by Rickettsiae. Respiratory tract infections caused by Mycoplasma pneumoniae. Lymphogranuloma venereum caused by Chlamydia trachomatis. Psittacosis (Ornithosis) due to Chlamydia psittaci. Trachoma caused by Chlam…

Important Warnings

WARNINGS MINOCYCLINE HYDROCHLORIDE TABLETS, LIKE OTHER TETRACYCLINE-CLASS ANTIBIOTICS, CAN CAUSE FETAL HARM WHEN ADMINISTERED TO A PREGNANT WOMAN. IF ANY TETRACYCLINE IS USED DURING PREGNANCY OR IF THE PATIENT BECOMES PREGNANT WHILE TAKING THESE DRUGS, THE PATIENT SHOULD BE APPRISED OF THE POTENTIAL HAZARD TO THE FETUS. THE USE OF DRUGS OF THE TETRACYCLINE CLASS DURING TOOTH DEVELOPMENT (LAST HALF…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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Other Minocycline Hydrochloride NDC Codes

13668-0484-05100 mg/1CAPSULE
2-Day
57664-0853-85100 mg/1CAPSULE
2-Day
13668-0484-50100 mg/1CAPSULE
2-Day
13668-0487-50100 mg/1TABLET
2-Day
67877-0438-30105 mg/1TABLET, FILM COATED, EXTENDED RELEASE
2-Day

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