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Cisplatin ndc

WebCisplatin is an antineoplastic agent that is FDA approved for the treatment of metastatic testicular tumors, metastatic ovarian tumors, and advanced bladder cancer. There is a Black Box Warning for this drug as shown here. Common adverse reactions include anemia, leukopenia, and thrombocytopenia . Adult Indications and Dosage WebDec 18, 2024 · Cisplatin is a platinum-based alkylating agent. It is labeled for use as a single agent for the treatment of advanced transitional cell bladder cancer, and in …

National Drug Code Directory - Food and Drug Administration

WebSep 15, 2024 · Cisplatin (Cisplatin Injection) may treat, side effects, dosage, drug interactions, warnings, patient labeling, reviews, and related medications including drug … WebProduct NDC: 16729-0288. Brand Name: Cisplatin. Generic Name: Cisplatin. Dosage Form Name: Injection. Administration Route: how to say corpuscular https://thebrummiephotographer.com

Etoposide Capsule: Package Insert - Drugs.com

WebCisplatin was administered intravenously at a dose of 75 mg/m 2 approximately 30 minutes after Pemetrexed administration on Day 1 of each cycle, ... NDC number Pack style 100 mg/4 mL: NDC 16729-522- 64: Carton containing one (1) single-dose vial: 500 mg/20 mL: NDC 16729-522- 05: WebCisplatin, NDC@PEG, and cNDC@PEG were administered intravenously at an equivalent dose of 40 μg of platinum per mouse bearing an A431(++) xenograft tumor (n = 3 per group). The mice were sacrificed at 3, 6, 9, 12, and 24 h after a single injection. Then the tumors were excised, washed with cold PBS, dried on filter paper, and weighed. WebGeneric Drug Code. 38920. Generic Drug Name. Cisplatin, Preservative Free. NDC Number. 00703574711. Product Dating. McKesson Acceptable Dating: we will ship >= … how to say corruption in japanese

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Cisplatin ndc

National Drug Code Directory - Food and Drug Administration

WebRecommended Dose: 500 mg/m^2 as an intravenous infusion over 10 minutes on Day 1 of each 21-day cycle, administered as a single agent or with cisplatin, in patients with creatinine clearance of 45 mL/minute or greater. See full prescribing information for further detail. For Medicaid and NC Health Choice Billing

Cisplatin ndc

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WebApr 25, 2024 · The NDC can be specifically internalized into EGFR positive cancer cells, resulting in higher therapeutic effect and lower side-effects relative to cisplatin. The Gd-binding domain enables the in situ detection of the drug distribution in vivo. MeSH terms Animals Antineoplastic Agents / chemistry Webfollowed by cisplatin 75 mg/m. 2 (both on day 1 only) followed by fluorouracil 750 mg/m. 2. per day as a 24-hour IV (days 1 to 5), starting at end of cisplatin infusion (2.4) SCCHN: 75 mg/m. 2followed by cisplatin 75 mg/m IV (day 1), followed by fluorouracil 750 mg/m2 per day as a 24 -hour IV (days 1 to 5), starting at end

WebApr 21, 2024 · A randomized controlled trial compared six cycles of cyclophosphamide 1000 mg/m 2, and cisplatin 100 mg/m 2 with or without Amifostine for Injection pretreatment at 910 mg/m 2, in two successive cohorts of 121 patients with advanced ovarian cancer. WebCisplatin is also sometimes used to treat head and neck cancer (including cancer of the mouth, lip, cheek, tongue, palate, throat, tonsils, and sinuses), lung cancer, cancer of the …

WebMar 22, 2024 · Use of cisplatin therapy is associated with reduced total body clearance. In children, elevated serum SGPT levels are associated with reduced drug total body clearance. Prior use of cisplatin may also … WebIn patients whose tumors are deemed unresectable after 2 cycles of cisplatin monotherapy, to determine the proportion of tumors rendered completely resectable by an additional 2 or 4 cycles of chemotherapy. (Group B) VI. To compare in a randomized fashion, EFS in patients with intermediate risk HB treated with 6 cycles of cisplatin/5 ...

WebApr 15, 2015 · CanMED: NDC. The Cancer Medications Enquiry Database (CanMED) is a two-part resource for cancer drug treatment related studies. ... Name: Cisplatin Strength: 1.0 Unit: mg/mL Packages: Code: 44567-0511-01 Description: 1 VIAL, MULTI-DOSE in 1 ...

WebFeb 1, 2024 · The molecular formula for Vincristine Sulfate, USP is C 46 H 56 N 4 O 10 ∙H 2 SO 4. It has a molecular weight of 923.04. The structural formula is as follows: Vincristine Sulfate, USP is a white to off–white powder. It is soluble in methanol, freely soluble in water, but only slightly soluble in 95% ethanol. how to say cosetteWebFeb 20, 2024 · Non-Small Cell Lung Cancer Recommended Dose and Schedule 28-day schedule The recommended dosage of Gemzar is 1000 mg/m 2 intravenously over 30 minutes on Days 1, 8, and 15 of each 28-day cycle in combination with cisplatin 100 mg/m 2 administered intravenously on Day 1 after Gemzar administration. 21-day schedule how to say corrinaWebNDC HCPCS Product NDC: 68001-0283 Brand Name: Cisplatin Generic Name: Cisplatin Dosage Form Name: Injection Administration Route: Intravenous Substances: Name: Cisplatin Strength: 1.0 Unit: mg/mL Packages: Code: 68001-0283-27 Description: 1 VIAL in 1 CARTON (68001-283-27) / 50 mL in 1 VIAL (68001-283-24) Effective Date: Aug. 2, … how to say corrugatedWebApr 3, 2024 · Cisplatin was administered intravenously at a dose of 75 mg/m 2 approximately 30 minutes after pemetrexed for injection administration on Day 1 of each cycle, ... NDC 63323-134-10 134010 PEMEtrexed. for Injection, USP 100 mg per vial. For intravenous use only. Caution: Cytotoxic Agent. Single-Dose Vial how to say coryzaWebAug 1, 2024 · Non-Squamous Non-Small Cell Lung Cancer (NSCLC) Alimta ® is indicated: in combination with pembrolizumab and platinum chemotherapy, for the initial treatment of patients with metastatic non-squamous non-small cell lung cancer (NSCLC), with no EGFR or ALK genomic tumor aberrations. northgatehrpensionsWebSep 27, 2024 · Cisplatin for injection, USP, a platinum-based drug for intravenous use, is a white to light yellow lyophilized powder. Each vial of Cisplatin for injection, USP … how to say corynebacteriumWebApr 13, 2024 · Trodelvy is approved under accelerated approval based on the objective response rate (ORR) and duration of response (DoR) established in Cohort 1. Cohorts 2, 3, 4 and 5 of the study are ongoing. Cohort 2 is assessing the safety and efficacy of Trodelvy monotherapy in platinum-ineligible patients after progression on anti-PD-1/PD-L1-based ... northgate hris