CCF(ALL-IN-ONE) TAB
Paracetamol + Guaiphenesin + Phenylephrine Hydrochloride + Cetirizine Dihydrochloride + Ambroxol Hydrochloride
10*10BLISTERHover to zoom · click to enlarge
| Composition | Febuxostat Tablets 80 mg |
|---|---|
| Packing | 10*10ALU |
| SHELF LIFE | 24 MONTHS |
| HSN CODE | 3004 |
| Category | Tablets |
| Supply | Wholesale & Export |
Dosage form: Film-coated tablet
Strength: 80 mg
Active ingredient: Febuxostat
Febuxostat — 80 mg per tablet
Febuxostat is the pharmacologically active component of Febuco-80. It belongs to the xanthine oxidase inhibitor class.
Its main action is to inhibit the enzyme xanthine oxidase, which is involved in the conversion of:
Hypoxanthine → Xanthine → Uric acid
By reducing xanthine oxidase activity, febuxostat decreases the production of uric acid, thereby lowering serum uric-acid concentrations.
The 80 mg designation means that each tablet contains 80 mg of febuxostat.
The package states:
“Excipients — q.s.”
Here, q.s. = quantum sufficiens, meaning quantity sufficient to manufacture the tablet to the required specifications.
Excipients are inactive ingredients and may perform functions such as:
Giving the tablet its required size and shape
Providing adequate mechanical strength
Helping the tablet disintegrate and release the active ingredient
Improving manufacturing and compression
Maintaining stability
Providing the film coating and its physical properties
Important: The supplied blister/pack does not list the individual excipients or their quantities, so their specific names cannot be reliably provided from this image.
The pack specifically states:
“Colour: Titanium Dioxide IP”
Titanium dioxide is used as a white pigment/opacifying agent, particularly in pharmaceutical tablet coatings.
Its purposes can include:
Giving the tablet coating a white, uniform appearance
Improving opacity
Helping provide a consistent visual appearance
Providing some protection of the tablet from light exposure
IP indicates that the ingredient conforms to the applicable Indian Pharmacopoeia standard.
A detailed way of writing the composition from the pack is:
Each film-coated tablet contains:
Febuxostat IP/BP — 80 mg
Excipients — q.s.
Colour — Titanium Dioxide IP
Dosage — As directed by the physician.
The image itself clearly establishes Febuxostat 80 mg, excipients q.s., and Titanium Dioxide IP. It does not provide enough information to identify the complete excipient formula.
The 80 mg refers to febuxostat, not to the total weight of the tablet.
The finished tablet will weigh more than 80 mg because it also contains the inactive excipients and coating materials.
For example:
Total tablet weight = Febuxostat 80 mg + excipients + coating components
The exact total tablet weight is not stated on the supplied packaging.
The composition is designed primarily to lower elevated uric-acid levels.
Febuxostat inhibits xanthine oxidase → reduces uric-acid synthesis → lowers circulating uric acid.
It is therefore used in the management of hyperuricemia associated with gout, according to the prescribing indication.
Note: Febuco-80 is a prescription medicine. The dose and duration should be determined by a physician, particularly because febuxostat treatment has important considerations involving cardiovascular history, liver function, kidney function, and other medicines.
Paracetamol + Guaiphenesin + Phenylephrine Hydrochloride + Cetirizine Dihydrochloride + Ambroxol Hydrochloride
10*10BLISTER