Veterinary medicinal product register

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Data selected by 1178 Name mastijet forte

Original name

Strength

Marketing authorisation number

Marketing authorisation holder:

ATCvet code

Species

Mastijet Forte

V/NRP/96/0344

Intervet International B.V., Nīderlande

QJ51RV01

lactating cows

Vairāk

Medicinal product information

Pharmaceutical form:	intramammary suspension
International name (active substance):	Bacitracin,Neomycin,Prednisolone,Tetracycline hydrochloridum
Distribution category:	To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release	Intervet International Booxmer, Nīderlande
Date of authorisation/renewal:	21-Mar-2011
Marketing authorisation valid until:	Unlimited time period
Marketing authorisation procedure:	NRP
Package leaflet:	[PDF] Skat_sadaļā_Zāļu_apraksts (17-May-2018)
Labelling text:	[PDF] Skat_sadaļā_Zāļu_apraksts (17-May-2018)
Summary of product characteristics:	[DOCX] Zāļu_informācija_ZA_M_LI (30-May-2023)

ID	Strength	Package size	Primary packaging	Labelling
V/NRP/96/0344-01		20	Injektors, 1 deva	[PDF] [PDF]

Mastijet Forte

V/I/21/0068

Intervet International BV, Nīderlande

QJ51RV01

lactating cows

Pharmaceutical form:	intramammary suspension
International name (active substance):	Tetracycline, Neomycin, Bacitracin, Prednisolone
Distribution category:	To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release	Intervet International Booxmer, Nīderlande
Date of authorisation/renewal:	09-Nov-2021
Marketing authorisation valid until:	08-Nov-2026
Marketing authorisation procedure:	I
Package leaflet:	[DOCX] Mastijet_Forte_PL_2023_06 (06-Jul-2023)
Labelling text:	See products section
Summary of product characteristics:	-

ID	Strength	Package size	Primary packaging	Labelling
V/I/21/0068-01		20	Polipropilēna šļirce, 8 g	[PDF]

Mastijet Forte

V/I/21/0043

Intervet International BV, Nīderlande

QJ51RV01

lactating cows

Vairāk

Pharmaceutical form:	intramammary suspension
International name (active substance):	Neomycin, Tetracycline hydrochloridum, Bacitracin, Prednisolone
Distribution category:	To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release	Intervet International Booxmer, Nīderlande
Date of authorisation/renewal:	19-Jun-2021
Marketing authorisation valid until:	18-Jun-2026
Marketing authorisation procedure:	I
Package leaflet:	[DOCX] 27072023_LI (27-Jul-2023)
Labelling text:	See products section
Summary of product characteristics:	-

ID	Strength	Package size	Primary packaging	Labelling
V/I/21/0043-01		20	Polipropilēna šļirce, 8 g	[PDF] [PDF]

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