SENTRY CAPGUARD nitenpyram tablet United States - English - NLM (National Library of Medicine)

sentry capguard nitenpyram tablet

sergeant's pet care products inc. - capguard™ tablets contain 11.4 or 57.0 mg of nitenpyram, which belongs to thechemical class of neonicotinoids. nitenpyram kills adult fleas. -

NITENPYRAM capsule United States - English - NLM (National Library of Medicine)

nitenpyram capsule

sergeant's pet care products inc. - nitenpyram (unii: 3a837vz81y) (nitenpyram - unii:3a837vz81y) -

Vanguard CPV. Ireland - English - HPRA (Health Products Regulatory Authority)

vanguard cpv.

zoetis belgium s.a. - live canine parvovirus strain nl-35-d - solution for injection - . - canine parvovirus - dogs - immunological - live vaccine

VANGUARD CPV-L. Ireland - English - HPRA (Health Products Regulatory Authority)

vanguard cpv-l.

zoetis belgium s.a. - live canine parvovirus strain nl-35-d; inactivated leptospira canicola; inactivated leptospira icterohaemorrhagiae - solution for injection - . - live canine parvovirus + inactivated leptospira - dogs - immunological - mixed vaccine (l & a)

Apiguard New Zealand - English - Ministry for Primary Industries

apiguard

vita (europe) limited - thymol - thymol 250 g/kg - miticide

VANGUARD 7. Ireland - English - HPRA (Health Products Regulatory Authority)

vanguard 7.

zoetis belgium s.a. - canine distemper virus strain n-cdv (live, attenuated); canine adenovirus type 2 virus, strain manhattan (live, attenuated); canine parainfluenza type 5 virus, strain nl-cpi-5 (live, attenuated); canine parvovirus strain nl-35-d (live, attenuated); leptospira canicola inactivated ; leptospira icterohaemorrhagiae inactivated - lyophilisate and solvent for solution for injection - . - live canine distemper virus + live canine adenovirus + live canine parainfluenza virus + live canine parvovirus + inactivated leptospira - dogs - immunological - mixed vaccine (l & a)

Vanguard Lepto-ci Ireland - English - HPRA (Health Products Regulatory Authority)

vanguard lepto-ci

zoetis belgium s.a. - leptospira icterohaemorrhagiae inactivated; leptospira canicola inactivated - solution for injection - . - leptospira - dogs - immunological - inactivated vaccine

Vanguard DA360 Tibial Tray - Uncoated knee tibia prosthesis, metallic Australia - English - Department of Health (Therapeutic Goods Administration)

vanguard da360 tibial tray - uncoated knee tibia prosthesis, metallic

zimmer biomet pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - cobalt chrome alloy tibial tray is for cemented use features 25 mm tapered stem boss which accepts offset stem adapters, stem extensions and cruciate wing augments. the superior surface features a cylindrical post that blends into a distal cone which is designed to mate with the vanguard da 360 tibial bearing. the seven symmetrical baseplate sizes in 4 mm m/l increments. packaged with ti/uhmwpe screw. cobalt chrome alloy tibial tray is a component of vanguard ssk 360 revision knee system. indications for use: painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved; correction of varus, valgus, or posttraumatic deformity; correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.

Vanguard DA360 Tibial Bearing - Prosthesis, knee, internal, insert component Australia - English - Department of Health (Therapeutic Goods Administration)

vanguard da360 tibial bearing - prosthesis, knee, internal, insert component

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - direct compression moulded uhmwpe arcom tibial mobile bearing. bi-helical articulation with the vanguard 360da tibial tray. deeper anterior cutout and one degree of varus/valgus lift off and does not limit the internal/ external rotation. direct compression moulded uhmwpe arcom mobile bearing. indications for use: painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved; correction of varus, valgus, or posttraumatic deformity; correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.