Prescription Drug Information: MINOCYCLINE HYDROCHLORIDE

MINOCYCLINE HYDROCHLORIDE- minocycline hydrochloride capsule
DirectRX

SPL Unclassified

Rx only

To reduce the development of drug-resistant bacteria and maintain the effectiveness of minocycline hydrochloride capsules, USP and other antibacterial drugs, minocycline hydrochloride capsules, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.

Description

Clinical Pharmacology

Contraindications

Warnings

Precautions

Adverse Reactions

Overdosage

Dosage and Administration

Animal Pharmacology and Toxicology

Patient Information

270
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MINOCYCLINE HYDROCHLORIDE
minocycline hydrochloride capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:61919-270(NDC:13668-484)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MINOCYCLINE HYDROCHLORIDE (MINOCYCLINE) MINOCYCLINE 100 mg
Inactive Ingredients
Ingredient Name Strength
MAGNESIUM STEARATE
STARCH, CORN
FERROSOFERRIC OXIDE
SHELLAC
GELATIN
POTASSIUM HYDROXIDE
TITANIUM DIOXIDE
PROPYLENE GLYCOL
Product Characteristics
Color gray (gray opaque cap, white opaque body) Score no score
Shape CAPSULE Size 18mm
Flavor Imprint Code RX696
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:61919-270-20 20 CAPSULE in 1 BOTTLE None
2 NDC:61919-270-30 30 CAPSULE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA065062 03/14/2018
Labeler — DirectRX (079254320)
Establishment
Name Address ID/FEI Operations
DirectRX 079254320 repack (61919-270)

Revised: 06/2022 DirectRX

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