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Nahaltin - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Nahaltin
Approved
STANDARD
Nahaltin
CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
e657c29cc88eb838
Company
CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.
Type
Standard
Approval Details
Approval Id
e657c29cc88eb838
Drug Approval Philippines Name
Nahaltin
Product Name
Nahaltin
Registration Number
DRP-6801
Brand Name
Nahaltin
Generic Name
Co-Amoxiclav
Dosage Form
Powder For Injection (Iv)
Dosage Strength
1g/200mg
Manufacturer
CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.
Importer
Sahar International Trading, Inc.
Distributor
Dynasty Pharmaceuticals
Company Detail Path
/organization/cspc-zhongnuo-pharmaceutical-shijiazhuang-co-ltd
Issuance Date
28 August 2023
Expiry Date
13 September 2028
Pharmacologic Category
Antibacterial (Penicillin)
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
e657c29cc88eb838
Type
Standard
Back to Philippines FDA Approvals