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active substance

Altrenogest — veterinary medicines

Authorised animal medicines containing Altrenogest across national registers. Regulatory residue limits (MRL) and antimicrobial-resistance surveillance are shown when on record. This is a neutral reference and does not provide dosing or veterinary advice.
Reference information only — not veterinary advice and not a dosing source. Always consult a licensed veterinarian before giving any medicine to an animal.

Target species

TruieChevalCerdas nulíparasCerdas jóvenesCerdas reproductorasSwine (pigs)HorsesPigs

Authorised products

63 authorised products across national registers.

United States — DailyMed (NLM)

Italy — Ministero della Salute

Residue limits (MRL)

Species: Equidae

1 μg/kg

European Union

Species: Equidae · Tissue: Fat

Marker residue: Altrenogest

Therapeutic class: Agents acting on the reproductive system

Species: Equidae

0.9 μg/kg

European Union

Species: Equidae · Tissue: Liver

Marker residue: Altrenogest

Therapeutic class: Agents acting on the reproductive system

Species: Porcine

0.4 μg/kg

European Union

Species: Porcine · Tissue: Liver

Marker residue: Altrenogest

Therapeutic class: Agents acting on the reproductive system

Species: Porcine

1 μg/kg

European Union

Species: Porcine · Tissue: Skin and fat

Marker residue: Altrenogest

Therapeutic class: Agents acting on the reproductive system

Species: Swine

4 ppb

United States

Species: Swine · Tissue: Liver (target tissue)

Species: Swine

1 ppb

United States

Species: Swine · Tissue: Muscle

Antimicrobial resistance surveillance

No antimicrobial-resistance surveillance is recorded for this substance.

Reported adverse events (openFDA)

Spontaneous adverse-event reports that name Altrenogest, by species — reported counts, not proven reactions.

Horse

53 reported events

openFDA

Top reactions: INEFFECTIVE, ESTRUS SUPPRESSIO (30) · Lack of efficacy - NOS (22) · Drug administration duration too long (17) · Mammary gland disorder NOS (11) · Mammary gland oedema (11)

Source: openFDA Animal & Veterinary adverse-event reports.

Surveillance reference only — these are spontaneous adverse-event report counts, not proven adverse reactions, not causation and not a measure of any product's risk or safety. Always consult a licensed veterinarian.

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