Calcium chloride; dextrose; magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium lactate - Generic Drug Details
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What are the generic drug sources for calcium chloride; dextrose; magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium lactate and what is the scope of freedom to operate?
Calcium chloride; dextrose; magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium lactate
is the generic ingredient in one branded drug marketed by Baxter Hlthcare and is included in one NDA. Additional information is available in the individual branded drug profile pages.Summary for calcium chloride; dextrose; magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium lactate
US Patents: | 0 |
Tradenames: | 1 |
Applicants: | 1 |
NDAs: | 1 |
Clinical Trials: | 75 |
DailyMed Link: | calcium chloride; dextrose; magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium lactate at DailyMed |
Recent Clinical Trials for calcium chloride; dextrose; magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium lactate
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Emory University | Phase 4 |
Makerere University | Phase 4 |
University of Maryland, Baltimore | Phase 4 |
US Patents and Regulatory Information for calcium chloride; dextrose; magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium lactate
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Baxter Hlthcare | PLASMA-LYTE M AND DEXTROSE 5% IN PLASTIC CONTAINER | calcium chloride; dextrose; magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium lactate | INJECTABLE;INJECTION | 017390-001 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |