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Buprigesic Bupre/norphine Hydrochloride I.P 0.3 mg
Buprigesic Bupre/norphine Hydrochloride I.P 0.3 mg

Buprigesic Bupre/norphine Hydrochloride I.P 0.3 mg

Buprigesic Bupre/norphine Hydrochloride I.P 0.3 mg Specification

  • Dosage Form
  • Injection
  • Pacakaging (Quantity Per Box)
  • 10 ampoules per box
  • Origin of Medicine
  • India
  • Indication
  • Pain management, opioid dependence
  • Salt Composition
  • Buprenorphine Hydrochloride 0.3 mg
  • Drug Type
  • Prescription Only (Rx)
  • Ingredients
  • Buprenorphine Hydrochloride I.P.
  • Physical Form
  • Injection
  • Function
  • Analgesic (pain relief)
  • Recommended For
  • Moderate to severe pain and as an adjunct in anesthesia
  • Dosage
  • As prescribed by the physician
  • Dosage Guidelines
  • Administer under medical supervision only
  • Suitable For
  • Adults
  • Quantity
  • 0.3 mg
  • Storage Instructions
  • Store below 30°C, protected from light and moisture
  • Packaging Type
  • Ampoules
  • Usage
  • For hospital or clinical use only
  • Shelf Life
  • 24 months from the date of manufacture
  • Appearance
  • Clear, colorless liquid
  • Route of Administration
  • Intramuscular (IM) or slow intravenous (IV) injection
  • Prescription Required
  • Yes
  • ATC Code
  • N02AE01
  • Medicine Strength
  • 0.3 mg per ampoule
  • Schedule
  • Schedule H Narcotic
 

Buprigesic Bupre/norphine Hydrochloride I.P 0.3 mg Trade Information

  • Minimum Order Quantity
  • 100 Units
  • Supply Ability
  • 1000 Per Day
  • Delivery Time
  • 7 Days
  • Sample Available
  • Yes
  • Sample Policy
  • Contact us for information regarding our sample policy
 

About Buprigesic Bupre/norphine Hydrochloride I.P 0.3 mg

Strength
0.3 mg /ml
Brand
Buprigesic
Manufrature
Neon Laboratories Limited
Shelf Life
36 month
Specification
Buprenorphine Hydrochloride I.P 0.3 mg
Country of Origin
Made in India
Minimum Order Quantity
100
Buprigesic 0.3mg Injection:An Effective Solution for Pain Management and Opioid Dependence


Precise Pain Relief for Hospital Settings

Buprigesic 0.3 mg delivers effective analgesia for moderate to severe pain, ensuring patient comfort under medical supervision. Its rapid onset and flexible administration routes (IM or IV) make it a preferred choice for clinicians in both surgical and emergency scenarios. Strict adherence to dosage protocols supports safe, targeted therapy.


Secure and Regulatory-Compliant Packaging

Each box contains 10 ampoules, protected to maintain integrity and potency for up to 24 months. Ampoule packaging simplifies storage and transport for hospital pharmacies, ensuring medications remain protected from light and moisture under recommended conditions.


Clinical Usage and Safety Assurance

This formulation is suitable exclusively for adult patients in hospital settings. Administration must be performed by healthcare professionals, with exact dosing individualized as per physician instructions. Prescribing and handling follow Schedule H Narcotic regulations to prevent misuse and ensure safety.

FAQ's of Buprigesic Bupre/norphine Hydrochloride I.P 0.3 mg:


Q: How should Buprigesic Buprenorphine Hydrochloride Injection be administered?

A: Buprigesic 0.3 mg ampoule is administered via intramuscular (IM) or slow intravenous (IV) injection by qualified medical personnel. Always follow the physician's instructions for dosage and technique.

Q: What indications does Buprigesic address in clinical practice?

A: Buprigesic is recommended for managing moderate to severe pain, often after surgery or injury, and is also used as a supplementary agent in anesthesia. It may be prescribed in hospital settings for opioid dependence where medically appropriate.

Q: When is Buprigesic injection appropriate for use?

A: This medication is administered when acute pain relief is required in adults, particularly in hospital or clinical environments. Use is determined by a physician based on patient needs and clinical guidelines.

Q: Where should Buprigesic ampoules be stored to ensure efficacy?

A: Store Buprigesic ampoules below 30C, protected from light and moisture. Pharmacy areas should comply with manufacturer recommendations to preserve product quality and shelf life.

Q: What is the process for obtaining Buprigesic Buprenorphine Hydrochloride Injection?

A: As a Schedule H Narcotic, Buprigesic requires a valid prescription and is dispensed only to recognized medical facilities or licensed professionals. Importers, exporters, manufacturers, and suppliers in India follow strict regulatory controls for distribution.

Q: What are the benefits of using Buprigesic in hospital pain management?

A: Buprigesic provides effective and rapid pain relief with controllable dosing, reducing patient discomfort. Its use under supervision minimizes adverse effects, improves safety, and optimizes postoperative and acute pain outcomes.

Q: Is Buprigesic suitable for everyone?

A: Buprigesic is formulated for adult patients and should be used only under direct medical supervision. It is not intended for pediatric use or for any purpose outside medical prescription and controlled settings.

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