GENERIC NAME OF THE MEDICINAL PRODUCT:

A. Amoxycillin and Potassium Clavulanate Injection IP 1.2g
B. Amoxycillin and Potassium Clavulanate Injection IP 600mg
C. Amoxycillin and Potassium Clavulanate Injection IP 300mg
D. Amoxycillin and Potassium Clavulanate Injection IP 150mg

QUALITATIVE AND QUANTITATIVE COMPOSITION:

A) Amoxycillin and Potassium Clavulanate Injection IP 1.2g
a) Each Vial Contains:
(Sterile) Amoxycillin Sodium IP
Eq. to Amoxycillin……………….…….1000mg
(Sterile) Potassium Clavulanate IP
Eq. to Clavulanic acid……………….…200mg
b) Sterile water for injection IP …………...20ml

B) Amoxycillin and Potassium Clavulanate Injection IP 600mg
a) Each Vial Contains:
(Sterile) Amoxycillin Sodium IP
Eq. to Amoxycillin……………….…….500mg
(Sterile) Potassium Clavulanate IP
Eq. to Clavulanic acid……………….…100mg
b) Sterile water for injection IP ………...10ml

C) Amoxycillin and Potassium Clavulanate Injection IP 300mg
a) Each Vial Contains:
(Sterile) Amoxycillin Sodium IP
Eq. to Amoxycillin……………….…….250mg
(Sterile) Potassium Clavulanate IP
Eq. to Clavulanic acid……………….…50mg
b) Sterile water for injection IP ………...10ml


D) Amoxycillin and Potassium Clavulanate Injection IP 150mg
a) Each Vial Contains:
(Sterile) Amoxycillin Sodium IP
Eq. to Amoxycillin……………….…….125mg
(Sterile) Potassium Clavulanate IP
Eq. to Clavulanic acid……………….…25mg
b) Sterile water for injection IP ………...5ml

THERAPEUTIC INDICATIONS:

The combination of amoxycillin and clavulanic acid is used to treat certain infections caused by bacteria, including infections of the ears, lungs, sinus, skin, and urinary tract. Amoxicillin is in a class of medications called penicillin-like antibiotics.

DIRECTION OF USE:

Reconstitute using 20ml or 10ml of SWFI.
Reconstituted solution should be used immediately after preparation.
Read the enclosed leaflet before reconstitution and use.

CAUTION AND SCHEDULE:

CAUTION: If any foreign particle is visible in the vial after dissolving the contents, please do not use the solution and return the vial for free replacement.
WFI IP Ampule is not manufactured by us.
Not for Intramuscular use.
Discard unused portion.
FLIP-OFF SEAL IS PROVIDED FOR TAMPER EVIDENCE
SCHEDULE: SCHEDULE H PRESCRIPTION DRUG-CAUTION: To be sold by retail on the prescription of Registered Medical Practitioner only.
NOT TO BE SOLD WITHOUT WATER FOR INJECTION.

STORAGE & DOSAGE:

STORAGE: Store protected from moisture. Do not freeze.
KEEP OUT OF REACH OF CHILDREN
For indications, dosage and administration, see enclosed leaflet.
DOSAGE: As directed by Physician.

Amoxycillin and Potassium Clavulanate Injection IP 300mg Technical Specification: 

Product Name:Amoxycillin and Potassium Clavulanate Injection IP 300mg
Brand Name:Clavuxan CV
Strength:1.2g, 600mg, 300mg, 150mg
Dosage Form:Lyophilized Powder for Injection (Sterile)
Packing:1 Vial + WFI in a Tray
Route of Administration:For I.V. use only
Pack Insert/Leaflet:PIL (Patient Information Leaflet)
Documents:COA, MOA, Product Permission, Stability Studies, GMP
Therapeutic use:β-lactam Antibiotic, Anti-bacterial & Penicillin.
Indication: The combination of amoxicillin and clavulanic acid is used to treat certain infections caused by bacteria. Amoxicillin is in a class of medications called penicillin-like antibiotics.
Storage:Store protected from moisture. Do not freeze.

GENERIC NAME OF MEDICINAL PRODUCT:

  • Amoxycillin and Potassium Clavulanate Injection IP 300mg

QUALITATIVE AND QUANTITATIVE COMPOSITION:

  • Amoxycillin and Potassium Clavulanate Injection IP 300mg
    Each Vial Contains:
    (Sterile) Amoxycillin Sodium IP
    Eq. to Amoxycillin……………….…….250mg
    (Sterile) Potassium Clavulanate IP
    Eq. to Clavulanic acid……………….…50mg
    Sterile water for injection IP ……………10ml

THERAPEUTIC INDICATION:

The combination of amoxycillin and clavulanic acid is used to treat certain infections caused by bacteria, including infections of the ears, lungs, sinus, skin, and urinary tract. Amoxicillin is in a class of medications called penicillin-like antibiotics.

DIRECTION OF USE:

Reconstitute using 20ml or 10ml of SWFI.

Reconstituted solution should be used immediately after preparation.

Read the enclosed leaflet before reconstitution and use.

CAUTION AND SCHEDULE:

CAUTION: If any foreign particle is visible in the vial after dissolving the contents, please do not use the solution and return the vial for free replacement.

WFI IP Ampule is not manufactured by us.
Not for Intramuscular use.

Discard unused portion.
FLIP-OFF SEAL IS PROVIDED FOR TAMPER EVIDENCE

SCHEDULE: SCHEDULE H PRESCRIPTION DRUG-CAUTION: To be sold by retail on the prescription of Registered Medical Practitioner only.

NOT TO BE SOLD WITHOUT WATER FOR INJECTION.

STORAGE AND DOSAGE:

STORAGE: Store protected from moisture. Do not freeze.

KEEP OUT OF REACH OF CHILDREN
For indications, dosage and administration, see enclosed leaflet.

DOSAGE: As directed by Physician.