Elementis Pharma
NDC Database
Elementis Pharma
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 14
- Latest Marketing Date 2013-11-12
- Data Source FDA
- First Marketing Date 2010-08-05
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Elementis Pharma
Giulinistraße 2, 67065 Ludwigshafen am Rhein
Germany
www.elementispharma.com/ olaf.schmitz@elementis.com View on MapNDC Records ( 14 records )
Nonproprietary Name
Aluminum Hydroxide Wet Gel
Dosage Form
GEL
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
ALUMINUM HYDROXIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-11-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Magaldrate
Dosage Form
GEL
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
MAGALDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-11-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ALUMINUM PHOSPHATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
ALUMINUM PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-08-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Hydrotalcite
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
HYDROTALCITE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-11-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Magaldrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
MAGALDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-11-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ALUMINUM HYDROXIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
ALUMINUM HYDROXIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-09-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SUCRALFATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
SUCRALFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-09-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sucralfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
SUCRALFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-09-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sodium Monofluorophosphate
Dosage Form
POWDER
Strength
25 kg/25kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
SODIUM MONOFLUOROPHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-03-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
DIHYDROXYALUMINUM SODIUM CARBONATE
Dosage Form
PASTE
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
DIHYDROXYALUMINUM SODIUM CARBONATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-08-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SUCRALFATE
Dosage Form
PASTE
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
SUCRALFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-09-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Magnesium Hydroxide
Dosage Form
PASTE
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
MAGNESIUM HYDROXIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-09-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aluminum Hydroxide
Dosage Form
PASTE
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
ALGELDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-09-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sucralfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Elementis Pharma Gmbh
Marketing Category
BULK INGREDIENT
Substance
SUCRALFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-11-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
14 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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Explore important National Drug Code information available in the records above.
NDC
55603-057
Nonproprietary Name
Aluminum Hydroxide Wet Gel
Labeler
Elementis Pharma Gmbh
Dosage Form
GEL
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