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SBCEF-TZ 1.125GM
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SBCEF-TZ 1.125GM Clinical Monograph & Batch COA

Certified DCGI Formulation Literature (PDF)

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InjectionPrescription Required (Schedule Drug)

SBCEF-TZ 1.125GM

Active Drug Composition

Ceftriaxone Sodium 1000mg + Tazobactam 125mg

WHO-GMP Certified Batch ManufacturingDCGI Approved Formulation100% BioavailableAlu-Alu Packaging

SBCEF-TZ 1.125GM (Ceftriaxone Sodium 1000mg + Tazobactam 125mg) is manufactured under strict WHO-GMP compliance for maximum bioavailability and therapeutic efficacy.

Dosage FormSterile Injectable (I.V. / I.M.)
Packaging PresentationSingle Dose Sterile Vial with Ampoule & WFI
B2B Distributor & Healthcare Professional Notice:This product is supplied solely through verified licensed pharmaceutical distributors, stockists, and institutional tenders. Online retail checkout for prescription formulations is legally restricted.

Clinical Pharmacology & Therapeutic Profile

Comprehensive therapeutic guidelines for medical practitioners and institutional procurement

Therapeutic Indications

Indicated for therapeutic management within specified clinical indications under qualified physician guidance.

Mechanism of Action (MOA)

The active pharmacological principles in SBCEF-TZ 1.125GM deliver targeted therapeutic action through standardized systemic bioavailability and verified pharmacodynamics.

Dosage & Posology

As directed by the registered medical practitioner. Strictly adhere to full course duration.

Safety & Precautions

Well tolerated under clinical supervision. Contraindicated in patients with hypersensitivity to active ingredients.

Storage Guidelines

Store between 2°C to 8°C or below 25°C as indicated on label. Protect from light.

WHO-GMP Certified Purity

Manufactured in state-of-the-art HVAC controlled cleanrooms with 100% active ingredient bio-potency and analytical batch testing.

Alu-Alu Moisture Barrier

Superior barrier protection against tropical humidity, preventing physical degradation and guaranteeing 24-month stability.

Exclusive District Monopoly

Strict PCD franchise monopoly allocation ensuring zero price competition and complete territory protection for our partners.

Technical Product Specifications

Therapeutic SegmentInjection
Dosage FormSterile Injectable (I.V. / I.M.)
Packaging TypeSingle Dose Sterile Vial with Ampoule & WFI
Regulatory ScheduleSchedule H1 Prescription Drug
Minimum Order Qty100 Units
Country of OriginIndia (Sidhpur Facility)
Quality StandardWHO-GMP & ISO 9001:2015
Batch Analytical COASupplied with Trade Invoice

Active Medical Composition

SBCEF-TZ 1.125GM features Ceftriaxone Sodium 1000mg + Tazobactam 125mg prepared to high pharmaceutical purity standards.

Therapeutic ClassificationInjection
Regulatory ScheduleSchedule Drug (Prescription Only)

*Disclaimer: Formulations are intended solely for distribution to licensed practitioners, hospitals, and pharmacies. Dosage must adhere to medical advice.

Monopoly PCD Franchise

Apply for Exclusive Marketing Rights of SBCEF-TZ 1.125GM

Check vacant territory availability in your state or district. Enjoy full marketing kit support, visual aids, and guaranteed zero competitor supply.

Distributor Inquiries

Questions Regarding SBCEF-TZ 1.125GM

What is the therapeutic indication and composition of SBCEF-TZ 1.125GM?

SBCEF-TZ 1.125GM contains Ceftriaxone Sodium 1000mg + Tazobactam 125mg indicated for Indicated for therapeutic management within specified clinical indications under qualified physician guidance. as formulated by Sygnus Biotech.

What packaging presentations are available for SBCEF-TZ 1.125GM?

SBCEF-TZ 1.125GM is supplied in tamper-evident Single Dose Sterile Vial with Ampoule & WFI, engineered with barrier foil protection to ensure a 24 to 36 month shelf life.

Is monopoly PCD franchise territory available for SBCEF-TZ 1.125GM?

Yes, Sygnus Biotech grants exclusive district-wise monopoly marketing rights for SBCEF-TZ 1.125GM along with promotional visual aids, product cards, and marketing support.

What is the regulatory schedule and minimum order quantity (MOQ)?

SBCEF-TZ 1.125GM is categorized as Schedule H1 Prescription Drug with an introductory PCD franchise MOQ of 100 units per batch.

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