Fareva
NDC Database
Fareva
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 23
- Latest Marketing Date 2022-06-23
- Data Source FDA
- First Marketing Date 1998-08-12
Company Overview
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Company Snapshot
Fareva
28 place de la gare, 1616 Luxembourg
Luxembourg
www.fareva.com/en CMiksch.excella@fareva.com View on MapNDC Records ( 23 records )
Nonproprietary Name
TEMSIROLIMUS
Dosage Form
INJECTION
Strength
25 mg/mL
Labeler
Fareva
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
TEMSIROLIMUS
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2020-12-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
BRENTUXIMAB VEDOTIN
Dosage Form
INJECTION
Strength
50 mg/10.5mL
Labeler
Fareva
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
BRENTUXIMAB VEDOTIN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2011-08-25
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
MYCOPHENOLATE MOFETIL
Dosage Form
INJECTION
Strength
500 mg/5mL
Labeler
Fareva
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
MYCOPHENOLATE MOFETIL
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
1998-08-12
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
CETRORELIX
Dosage Form
INJECTION
Strength
0.25 mg/mL
Labeler
Fareva
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
CETRORELIX
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2000-11-08
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
TRASTUZUMAB
Dosage Form
INJECTION
Strength
150 mg/6.36mL
Labeler
Fareva
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
TRASTUZUMAB
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2021-06-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
TRASTUZUMAB
Dosage Form
INJECTION
Strength
420 mg/17.6mL
Labeler
Fareva
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
TRASTUZUMAB
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2020-04-15
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Relebactam
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
RELEBACTAM ANHYDROUS
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-01-02
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Estradiol benzoate coarse grade
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
ESTRADIOL BENZOATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-10-18
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Estradiol benzoate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
ESTRADIOL BENZOATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-02-23
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Estradiol Hemihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
ESTRADIOL HEMIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-08-30
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Estradiol hemihydrate micronized fine grade
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
ESTRADIOL HEMIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-07-10
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Estradiol Valerate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
ESTRADIOL VALERATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-02-23
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Estradiol valerate micronized fine grade
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
ESTRADIOL VALERATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-04-07
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Hydrocortisone hemisuccinate monohydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
HYDROCORTISONE HEMISUCCINATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-08-30
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Norethindrone acetate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
NORETHINDRONE ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-05-04
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Norethindrone acetate micronized
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
NORETHINDRONE ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-09-21
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Norethindrone micronized
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
NORETHINDRONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-09-21
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Trazodone hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
TRAZODONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-04-15
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Trenbolone acetate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
TRENBOLONE ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2010-03-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Atrenogest
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
ALTRENOGEST
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-11-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Tenapanor
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
TENAPANOR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-06-22
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Avibactam Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
AVIBACTAM SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-06-22
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Estradiol Cypionate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Valdepharm
Marketing Category
BULK INGREDIENT
Substance
ESTRADIOL CYPIONATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-06-23
End Marketing Date
-
Listing Record Certified Through
2027-12-31
NDC Type Breakdown
23 total- Drug for Further Processing
- Bulk Ingredient
Official Source
NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).
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NDC
78848-002
Nonproprietary Name
TEMSIROLIMUS
Labeler
Fareva
Dosage Form
INJECTION
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