1. Home
  2. Resources
  3. Schedule H, H1 and X register basics
Guide

Schedule H, H1 and X register basics

Plain-language basics of Schedule H, H1 and X drug records for Indian pharmacies: what is recorded, retention, prescriptions and a safe-practice checklist. Not legal advice.

8 min readUpdated 23 Oct 2026India-specific

The three schedules in brief

The Drugs Rules, 1945 place certain drugs in schedules that restrict how they may be sold. In simple terms:

ScheduleWhat it generally means
HSold only on the prescription of a registered medical practitioner
H1A stricter list, including certain antibiotics and anti-TB drugs, with an additional register of sales
XNarcotic and psychotropic substances with the strictest controls, including prescription retention

Narcotic drugs and psychotropic substances are additionally governed by the NDPS Act and its rules, with their own licensing and registers.

What pharmacies usually record

For Schedule H1 and similar categories, the sale record typically includes the patient name and address, the prescriber’s name and registration details, the drug name, quantity and batch number, and the date. Confirm the exact fields required for your licence with your regulatory adviser.

Retention

Retention periods differ by schedule and rule. Commonly cited periods are about three years for Schedule H1 registers and about two years for Schedule X prescriptions, but you must confirm the current rule text and any state-specific requirement before relying on them.

Prescription handling

  • Check that the prescription is valid, dated and signed by a registered practitioner
  • Dispense only the quantity and strength prescribed
  • Where required, mark the prescription as dispensed with your pharmacy details and date
  • Do not accept altered or photocopied prescriptions where the rules disallow it
  • A registered pharmacist should supervise dispensing

How software helps

Software cannot make you compliant, but it can reduce missing entries: it can force doctor and patient fields on scheduled items, tie each sale to a batch, produce a register-style report and keep an audit log of edits. Review the report format with your adviser or inspector expectations in your state. See Curafisc compliance support.

Safe-practice checklist


See how Curafisc helps More guides

See Curafisc on your own data

Book a guided demo or join the early-access list. We will help you load a sample of your items and bills so you can judge the software on your real workflow.