This brand name is authorized in Nigeria.
The drug AFRABRON contains one active pharmaceutical ingredient (API):
1
|
UNII
UM5219H89V - IRON POLYMALTOSE
|
This drug has been approved in Nigeria as follows:
| Identifier | Form | Presentation | Description | Approval |
|---|---|---|---|---|
| A11-100077 | Syrup | Afrabron Syrup SYRUP 50 mg/5 mL 200 mL | Orange flavoured syrup Each 5 mL contains: Iron (III) Hydroxide Polymaltose Complex 166.6 mg equiv. to elemental Iron 50 mg Other ingredients: Sorbitol Liquid 70% (650 mg), Propylene Glycol 300 mg, Glycerol 1100 mg, Propyl Paraben 3.35 mg, Ethyl Paraben 0.375 mg, EDTA 0.5 mg, Orange Flavour 2.5 mg per 5 mL | 17/05/2021 |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| NG | Registered Drug Product Database | A11-100077 |
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