Best Tetracycline Capsule with GMP/BP/USP Supplier, Service

[Drug name]
Common name: tetracycline capsule
Trade name: tetracycline Capsule
English name: Tetracycline Capsules

[Composition and traits]
Main components: The main component of this product is tetracycline or tetracycline hydrochloride.
Character: This product is a capsule agent.

[indication]
It is used for ricettsiosis, mycoplasma infection, chlamydia infection, return fever, brucellosis, cholera, rabbit fever, plague, soft fever, and plague treatment in combination with aminoglycosides; but also for skin surface infections of conjunctivitis, blepharitis, keratitis, trachoma, etc. of sensitive pathogens or by Gram-positive bacteria and Gram-negative bacteria.

[Specifications and Packaging]
Single-dose specification: 250MG
Packaging specification: 10x10 grains

[usage and dosage]
profess to be convinced.
1. Adult dose: 250-500mg once, once every 6 hours.
2. Dosage for children: 25-50mg / kg a day, taken in four times.

[untoward effect]
1. Gastrointestinal symptoms such as nausea, vomiting, upper abdominal discomfort, abdominal distension, diarrhea, etc.
2. Abnormal reaction: mostly maculopapular and erythema, a few patients may appear urticaria, angionervous edema, allergic purpura, pericarditis and systemic lupus erythematosus rash aggravation, epidermal peeling dermatitis is not common.
3. Hematological system: occasionally can cause hemolytic anemia, thrombocytopenia, neutropenia and acidophilocytopenia.
4. Central nervous system: occasionally can cause benign intracranial pressure increase, can be manifested as headache, vomiting, optic nerve papilloedema, etc.
5. Nephrotoxicity: Patients with previously significant renal impairment may experience increased azacentraemia, hyperphosphataemia, and acidosis.

[taboo]
Patients with a history of tetracycline allergy are prohibited.

[matters need attention]
1. Cross-allergic reaction: People who are allergic to a tetracycline drug can be allergic to this product.
2. Interference to diagnosis: When determining the concentration of urinary catecholamine (Hingerty method), the measurement results can be high due to the interference of the product to fluorescence. This product can increase the determination value of alkaline phosphatase, blood urea nitrogen, serum amylase, serum bilirubin, serum amino transferase (AST, ALT).
3. Long-term medication should be regularly checked for blood routine and liver and kidney function.

[condition of storage]
Keep sealed below 25℃.
[term of validity]
24 Months

Product Description

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Frequently Asked Questions
What are GMP, BP, and USP standards for these products?
GMP (Good Manufacturing Practice), BP (British Pharmacopoeia), and USP (United States Pharmacopeia) are international quality standards that ensure pharmaceutical products are consistently produced and controlled according to strict quality regulations.
Are these medications suitable for international distribution?
Yes, these products are manufactured following international guidelines, making them suitable for healthcare systems and pharmacies globally, provided local registration requirements are met.
How should the injections and tablets be stored?
Generally, these pharmaceutical products should be stored in a cool, dry place, away from direct sunlight. Specific temperature requirements (such as "store below 25°C") are provided on the individual product packaging.
What is the difference between capsules and tablets in this range?
The choice between tablets (like Diclofenac or Abendazole) and capsules (like Piroxicam) often depends on the specific drug formulation and how it is intended to be absorbed by the body. Both forms are produced to high quality standards.
Is documentation available for regulatory registration?
Comprehensive documentation including COA (Certificate of Analysis) and other necessary dossiers can be provided to support the registration process in various international markets.
Can these products be used without a prescription?
These are pharmaceutical-grade medications. They should only be used under the guidance of a qualified healthcare professional and in accordance with local medical regulations.

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