Registered Owners
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ERRITA PHARMA
Jl. Peundeuy RT. 04/07 Desa Bojongsalam, Kec. Rancaekek, Jawa Barat, Indonesia
NPWP: 011041811441000
owner
Direktorat Registrasi ObatValid
RANITIDINE HYDROCHLORIDE
- BPOM Number
- GKL1606507417A1
- Approved
- 21 November 2024
- Expiry
- 11 October 2027
- Form
- TABLET SALUT SELAPUT; 167.41 MG
About This Registration
RANITIDINE HYDROCHLORIDE is a BPOM-registered direktorat registrasi obat in Indonesia, registered under number GKL1606507417A1. Its current registration status is Valid, with the licence valid until 11 October 2027. The product is registered to ERRITA PHARMA and manufactured by ERRITA PHARMA - INDONESIA. BPOM first approved this registration in October 2022. 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
- Registrasi Obat
- Packaging
- DUS, 10 STRIP @ 10 TABLET SALUT SELAPUT
- Department
- Direktorat Registrasi Obat
- Data Last Updated
- 13 November 2025
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Manufacturing Sites
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ERRITA PHARMA - INDONESIA
KAB. BANDUNG
primary
Ingredients (1)
RANITIDINE HYDROCHLORIDE
Market Intelligence
- Owner Portfolio
- ERRITA PHARMA holds 132 BPOM registrations
- Manufacturer Scale
- ERRITA PHARMA - INDONESIA produces 116 registered products
- Registration Age
- Registered for 3 years, 11 months
FDA Cross-Reference
via openFDA- Generic Name
- RANITIDINE
- Product Type
- HUMAN OTC DRUG
- Route of Administration
- ORAL
- Purpose
- Purpose Acid reducer
Data sourced from the U.S. FDA drug label database (openFDA). May not exactly match this product variant.
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