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Calcium Folinate - 0703-2797-01 - (Calcium Folinate)

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Drug Information of Calcium Folinate

Product NDC: 0703-2797
Proprietary Name: Calcium Folinate
Non Proprietary Name: Calcium Folinate
Active Ingredient(s): 10    mg/mL & nbsp;   Calcium Folinate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Calcium Folinate

Product NDC: 0703-2797
Labeler Name: Teva Parenteral Medicines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Start Marketing Date: 20110712

Package Information of Calcium Folinate

Package NDC: 0703-2797-01
Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-2797-01) > 30 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Calcium Folinate

NDC Code 0703-2797-01
Proprietary Name Calcium Folinate
Package Description 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-2797-01) > 30 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0703-2797
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcium Folinate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110712
Marketing Category Name UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Labeler Name Teva Parenteral Medicines, Inc
Substance Name LEUCOVORIN CALCIUM
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Folate Analog [EPC],Folic Acid [Chemical/Ingredient]

Complete Information of Calcium Folinate


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