Ciprofloxacin HCL USP is a highly potent broad-spectrum antibiotic approved by the FDA for comprehensive treatment of a wide range of bacterial infections. It is specifically formulated to combat urinary tract infections, sexually transmitted infections such as gonorrhea and chancroid, as well as skin, bone, and joint infections. Additionally, it is effective against prostatitis, typhoid fever, gastrointestinal infections, and lower respiratory tract infections. Ciprofloxacin HCL USP also serves as an essential treatment option for serious conditions like anthrax, plague, and salmonellosis. This antibiotic is produced following USP standards ensuring high purity and efficacy, making it an ideal choice for pharmaceutical manufacturers and healthcare providers requiring reliable anti-infective agents for their formulations or treatments.
Key Features
| Features | Description |
|---|---|
| Active Ingredient | Ciprofloxacin Hydrochloride USP |
| Spectrum | Broad-spectrum antibiotic effective against gram-negative and some gram-positive bacteria |
| FDA Approval | For treating multiple infections including urinary tract, respiratory, gastrointestinal, and sexually transmitted infections |
| Therapeutic Uses | Includes UTI, gonorrhea, chancroid, skin, bone, joint infections, prostatitis, typhoid fever, anthrax, plague, and salmonellosis |
| Purity Standard | USP (United States Pharmacopeia) certified |
| Formulation | Pharmaceutical raw material suitable for drug manufacturing |
| Packaging | Provided as a powder or granule form for pharmaceutical formulation |
| Storage Conditions | Store in a cool, dry place protected from light |
| Attributes | Description |
|---|---|
| Chemical Name | Ciprofloxacin Hydrochloride |
| CAS Number | 85721-33-1 |
| Molecular Formula | C17H18FN3O3·HCl |
| Molecular Weight | 385.82 g/mol |
| Appearance | White to off-white crystalline powder |
| Assay | ≥ 98% (HPLC method) |
| Solubility | Freely soluble in water and glacial acetic acid |
| USP Compliance | Meets all USP quality attributes including purity, identity, and potency |
| Intended Usage | For pharmaceutical manufacturing and formulation use only |
| Shelf Life | Minimum 24 months under recommended storage conditions |
*Disclaimer: The above description has been AI-generated and has not been audited or verified for accuracy. It is recommended to verify product details independently before making any purchasing decisions.
No, Ciprofloxacin HCL USP is a raw pharmaceutical ingredient intended solely for formulation and manufacturing of finished pharmaceutical products and must not be consumed directly.
While Ciprofloxacin HCL USP complies with USP standards, manufacturers must ensure the raw material also meets any additional Indian Pharmacopoeia (IP) requirements applicable.
Yes, Ciprofloxacin HCL USP can be used in veterinary antibiotic drug formulations subject to regulatory approvals and compliance.
Packaging is typically available in pharmaceutical-grade, moisture-proof containers with weight specifications tailored to manufacturing requirements.
The product guarantees a minimum purity of 98% as analyzed by validated HPLC methods according to USP standards.
Country Of Origin: India
Ciprofloxacin has FDA approval to treat urinary tract infections, sexually transmitted infections (gonorrhea and chancroid), skin, bone, joint infections, prostatitis, typhoid fever, gastrointestinal infections, lower respiratory tract infections, anthrax, plague, and salmonellosis.
