Direktorat Registrasi ObatValid

MELOXICAM

Claim this product
BPOM Number
GKL1718829110B1
Approved
27 June 2026
Expiry
2 June 2029
Form
Tablet

About This Registration

MELOXICAM is a BPOM-registered direktorat registrasi obat in Indonesia, registered under number GKL1718829110B1. Its current registration status is Valid, with the licence valid until 2 June 2029. The product is registered to OTTO PHARMACEUTICAL INDUSTRIES - INDONESIA. BPOM first approved this registration in April 2026. All registration data is sourced directly from the official BPOM public database and updated daily.

Registration data updated by BPOM

This product's registration details were changed on 30 June 2026. This may reflect a status change, renewal, or correction by BPOM.

Registration Details

Application
newaero
Packaging
DUS, 10 STRIP @ 10 TABLET
Department
Direktorat Registrasi Obat
Data Last Updated
30 June 2026

Retail Audit Service

Get detailed market intelligence for this product across Indonesian retail channels

Multiple cities available
Custom questionnaires
Professional shoppers
Detailed reporting
Starting from $50 per city
What's included in the audit service?

Stock availability and positioning verification

Price checking and competitor analysis

Display quality and promotional material assessment

Store condition and customer experience evaluation

Custom questions tailored to your research needs

Professional photographs and detailed reports

Registered Owners

  • OTTO PHARMACEUTICAL INDUSTRIES - INDONESIA

    KAB. BANDUNG BARAT

    NPWP: 011047750441000

    owner
    View profile →

Manufacturing Sites

Ingredients (1)

MELOXICAM

Market Intelligence

Owner Portfolio
OTTO PHARMACEUTICAL INDUSTRIES - INDONESIA holds 193 BPOM registrations
Manufacturer Scale
OTTO PHARMACEUTICAL INDUSTRIES - INDONESIA produces 193 registered products
Registration Age
Registered for 2 months
Update Status
Recently updated (20 days ago)

FDA Cross-Reference

via openFDA
Generic Name
MELOXICAM
Product Type
HUMAN PRESCRIPTION DRUG
Route of Administration
ORAL

Data sourced from the U.S. FDA drug label database (openFDA). May not exactly match this product variant.

Is this your product?

Claim it to manage registration, track renewals, and get expiry alerts.

Claim Product
1