National Drug Code (NDC) Database
Sotera Health LLC
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NDC:
70298-0670
-
Nonproprietary Name:
Medroxyprogesterone acetate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MEDROXYPROGESTERONE ACETATE
-
Start Marketing Date:
2019-09-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Specialized Rx Products, L. L. C.
-
NDC:
72467-200
-
Nonproprietary Name:
VersaPenn (AL) Anhydrous Lipid Base
-
Dosage Form:
CREAM
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 g/g
-
Substance:
TITANIUM DIOXIDE
-
Start Marketing Date:
2022-07-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Specialty Minerals Incorporated
-
NDC:
53004-3370
-
Nonproprietary Name:
Calcium Carbonate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CALCIUM CARBONATE
-
Start Marketing Date:
2003-01-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Spectrum Chemical and Laboratory Products
-
NDC:
49452-0032
-
Nonproprietary Name:
Fentanyl Citrate
-
Dosage Form:
CRYSTAL
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
FENTANYL CITRATE
-
Start Marketing Date:
1997-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CII
-
Certified Through:
2026-12-31
Spectrum Chemicals and Laboratory Product
-
NDC:
49452-7085
-
Nonproprietary Name:
Sodium Valproate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
VALPROATE SODIUM
-
Start Marketing Date:
2008-05-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Spectrum Chemicals and Laboratory Products
-
NDC:
49452-8255
-
Nonproprietary Name:
Bupropion Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
BUPROPION HYDROCHLORIDE
-
Start Marketing Date:
2009-04-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Spectrum Laboratory Products Inc
-
NDC:
49452-7401
-
Nonproprietary Name:
Sucralfate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SUCRALFATE
-
Start Marketing Date:
1998-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Spectrum Laboratory Products Inc.
-
NDC:
49452-4956
-
Nonproprietary Name:
Oxytocin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 mg/mg
-
Substance:
OXYTOCIN
-
Start Marketing Date:
2004-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Spectrum Laboratory Products, Inc
-
NDC:
49452-2011
-
Nonproprietary Name:
Cholestyramine Resin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
CHOLESTYRAMINE
-
Start Marketing Date:
1999-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
0406-9451
-
Nonproprietary Name:
Dextroamphetamine Sulfate Fine NP
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DEXTROAMPHETAMINE SULFATE
-
Start Marketing Date:
2025-08-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CII
-
Certified Through:
2026-12-31
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