Direktorat Registrasi ObatValid

AMLODIPINE BESILATE

BPOM Number: GKL1340100404A1
Approved: 16 March 2026
Expiry: 2 October 2030
Form: KAPLET

About This Registration

AMLODIPINE BESILATE is a BPOM-registered direktorat registrasi obat in Indonesia, registered under number GKL1340100404A1. Its current registration status is Valid, with the licence valid until 2 October 2030. The product is registered to HARBAT FARMA - INDONESIA. BPOM first approved this registration in February 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 13 November 2025. This may reflect a status change, renewal, or correction by BPOM.

Registration Details

Application: newaero
Packaging: DUS, 5 STRIP @ 10 KAPLET
Department: Direktorat Registrasi Obat
Data Last Updated: 13 November 2025

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

HARBAT FARMA - INDONESIA
KAB. TANGERANG
NPWP: 12345678910
owner
View profile →

Manufacturing Sites

HARBAT FARMA - INDONESIA
KAB. TANGERANG
primary
View profile →

Ingredients (1)

AMLODIPINE BESILATE

Market Intelligence

Owner Portfolio: HARBAT FARMA - INDONESIA holds 20 BPOM registrations
Manufacturer Scale: HARBAT FARMA - INDONESIA produces 20 registered products
Registration Age: Registered for 6 months

FDA Cross-Reference

via openFDA

Generic Name: AMLODIPINE BESYLATE
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?