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FSSAI MRLs (Veterinary)

FSSAI MRLs (Veterinary)

Author: KodiBook Digital Research Team
Editorial Review: KodiBook Editorial Team
Last Updated: 2026-06-27

Identity

Statutory Maximum Residue Limits (MRLs) established by the FSSAI that cap the allowed amount of therapeutic veterinary drug residues in consumable animal products.

Overview

Enacted by the Ministry of Health and Family Welfare under the Food Safety and Standards Act, 2006, these high-priority statutory limits dictate residue tolerances for veterinary drugs and absolute bans for prohibited substances. By regulating chemical presence in poultry meat and eggs, the rules enforce mandatory on-farm withdrawal periods to prevent human antimicrobial resistance and toxicity.

Structured Facts

Classification

Statutory Standards & Regulations

Purpose

To prevent antimicrobial resistance, toxicity, carcinogenicity, and allergenicity in human food chains by regulating veterinary medication residues.

Scope & Applicability

Applies to all consumable animal products, including poultry muscle, liver, kidney, fat, and avian eggs. Governs both therapeutic antibiotics and prohibited extraneous substances.

Regulatory Requirements

Mandates strict adherence to withdrawal periods for feed-grade medications and additives (e.g., Nicarbazin 24-hr, Tiamulin 72-hr, Maduramycin 5-7 days). Farm operators must cease administration prior to slaughter to ensure residues fall below MRLs.

Compliance Criteria

Detection of residues above permissible limits or detection of any prohibited substance constitutes a food safety violation.

Monitoring & Inspection

Compliance assessed through certified laboratory testing using HPLC-MS/MS equipment.

Documentation & Record Keeping

Requires logging treatment dates, dosages, and withdrawal periods in Medication Admin Logs.

Penalties / Non-Compliance

Violations trigger food safety prosecution and product recalls. High stocking densities causing stress can suppress immunity and lead to over-medication, raising compliance risks.

Best Practices

Implement improved biosecurity and hygiene to reduce reliance on antibiotics.

Quantitative Data

  • Maximum Permissible Limits: Tetracycline / Oxytetracycline / Chlortetracycline: 0.2 mg/kg (Muscle), 0.6 mg/kg (Liver), 1.2 mg/kg (Kidney), 0.4 mg/kg (Eggs). Erythromycin: 0.1 mg/kg (Muscle/Liver/Kidney/Fat), 0.05 mg/kg (Eggs). Neomycin: 0.5 mg/kg (Muscle/Liver/Fat/Eggs), 10.0 mg/kg (Kidney). Spectinomycin: 0.5 mg/kg (Muscle), 2.0 mg/kg (Liver/Fat/Eggs), 5.0 mg/kg (Kidney). Danofloxacin: 0.2 mg/kg or 0.1 mg/kg (Muscle/Fat), 0.4 mg/kg (Liver/Kidney). Amprolium: 0.5 mg/kg or 2.0 mg/kg (Muscle/Fat), 1.0 mg/kg or 7.0 mg/kg (Liver/Kidney/Eggs). Flumequine: 0.5 mg/kg or 1.0 mg/kg (Muscle/Liver/Fat), 3.0 mg/kg (Kidney). Ampicillin / Apramycin: 0.01 mg/kg (All Tissues/Fat). Cloxacillin / Clopidol: 0.01 mg/kg (All Tissues/Fat). Nicarbazin: 0.2 mg/kg (Muscle/Liver/Kidney/Fat). Pesticides (Default): 0.01 mg/kg.
  • Compliance Thresholds: HPLC-MS/MS testing must confirm a signal-to-noise ratio >= 3 for target product ion peaks and analyte retention times within ±5% of standard controls.
  • Unit: mg/kg

Relationships

  • Housing Systems: Stocking Density
  • Medicines: Poultry Medicines, Veterinary Residue Limits
  • Regulatory Authorities: Food Safety and Standards Authority of India (FSSAI), Ministry of Health and Family Welfare