UQUIFA
NDC Database
UQUIFA
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 19
- Latest Marketing Date 2025-11-10
- Data Source FDA
- First Marketing Date 2009-10-22
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UQUIFA
C/ Mallorca 262, 3rd floor, Barcelona 08008
Spain
uquifa.com/ ncaccamo@uquifa.com View on MapNDC Records ( 19 records )
Nonproprietary Name
Cimetidine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Union Quimico Farmaceutica SA
Marketing Category
BULK INGREDIENT
Substance
CIMETIDINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-10-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ranitidine Hydrochloride Form II
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Union Quimico Farmaceutica SA
Marketing Category
BULK INGREDIENT
Substance
RANITIDINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-10-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ranolazine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Union Quimico Farmaceutica SA
Marketing Category
BULK INGREDIENT
Substance
RANOLAZINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-01-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sitagliptin Phosphate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Union Quimico Farmaceutica SA
Marketing Category
BULK INGREDIENT
Substance
SITAGLIPTIN PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-01-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ranolazine Micronized
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Union Quimico Farmaceutica SA
Marketing Category
BULK INGREDIENT
Substance
RANOLAZINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-01-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bismuth Subcitrate Potassium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Union Quimico Farmaceutica SA
Marketing Category
BULK INGREDIENT
Substance
BISMUTH SUBCITRATE POTASSIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-09-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ketoconazole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
UNION QUIMICO FARMACEUTICA SA
Marketing Category
BULK INGREDIENT
Substance
KETOCONAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-11-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tropicamide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Union Quimico Farmaceutica SA
Marketing Category
BULK INGREDIENT
Substance
TROPICAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-11-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zolpidem Tartrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Uquifa Mexico, S.A. DE C.V.
Marketing Category
BULK INGREDIENT
Substance
ZOLPIDEM TARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
CIV
Start Marketing Date
2009-11-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Venlafaxine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
UQUIFA Mexico, S.A. DE C.V.
Marketing Category
BULK INGREDIENT
Substance
VENLAFAXINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-11-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levofloxacin Hemihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Uquifa Mexico, S.A. DE C.V.
Marketing Category
BULK INGREDIENT
Substance
LEVOFLOXACIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-11-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Rabeprazole Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
UQUIFA Mexico, S.A. DE C.V.
Marketing Category
BULK INGREDIENT
Substance
RABEPRAZOLE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-11-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
carisoprodol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
UQUIFA MEXICO, S.A. DE C.V.
Marketing Category
BULK INGREDIENT
Substance
CARISOPRODOL
Product Type
BULK INGREDIENT
DEA Schedule
CIV
Start Marketing Date
2012-10-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pregabalin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
UQUIFA Mexico, S.A. de C.V.
Marketing Category
BULK INGREDIENT
Substance
PREGABALIN
Product Type
BULK INGREDIENT
DEA Schedule
CV
Start Marketing Date
2014-11-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Cinacalcet HCI
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
UQUIFA Mexico, S.A. de C.V.
Marketing Category
BULK INGREDIENT
Substance
CINACALCET HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-11-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Telmisartan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
UQUIFA Mexico, S.A. de C.V.
Marketing Category
BULK INGREDIENT
Substance
TELMISARTAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-03-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Rivaroxaban
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Uquifa Mexico, S.A. de C.V.
Marketing Category
BULK INGREDIENT
Substance
RIVAROXABAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-10-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Oxantel Pamoate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Uquifa Mexico, S.A. de C.V.
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
OXANTEL PAMOATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Halofantrine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
UQUIFA Mexico, S.A. DE C.V.
Marketing Category
BULK INGREDIENT
Substance
HALOFANTRINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-11-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
19 total- 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
49711-0095
Nonproprietary Name
Cimetidine
Labeler
Union Quimico Farmaceutica SA
Dosage Form
POWDER
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