National Drug Code (NDC) Database
Focus Health Group, Inc
-
NDC:
24357-300
-
Nonproprietary Name:
Sterile Aluminum Potassium Sulfate
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
10 g/10g
-
Substance:
POTASSIUM ALUM
-
Start Marketing Date:
2025-03-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Formosa Laboratories, Inc.
-
NDC:
66499-0080
-
Nonproprietary Name:
XAV-939
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
XAV-939
-
Start Marketing Date:
2025-01-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Formulation Technology LLC
-
NDC:
53967-002
-
Nonproprietary Name:
MENTHOL
-
Dosage Form:
TABLET, EXTENDED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
10 mg/1
-
Substance:
MENTHOL
-
Start Marketing Date:
2026-02-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Foshan Nanhai Zhongnan Pharmaceutical Factory
-
NDC:
83626-001
-
Nonproprietary Name:
Methyl Salicylate
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
METHYL SALICYLATE
-
Start Marketing Date:
2023-07-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Fournier Laboratories Ireland LTD
-
NDC:
68543-3189
-
Nonproprietary Name:
Fenofibrate
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
145 mg/1
-
Substance:
FENOFIBRATE
-
Start Marketing Date:
2016-04-04
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
FRANCOPIA
-
NDC:
52465-107
-
Nonproprietary Name:
NALOXONE HYDROCHLORIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NALOXONE HYDROCHLORIDE
-
Start Marketing Date:
2020-07-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Fresenius Kabi AUT GmbH
-
NDC:
18124-009
-
Nonproprietary Name:
Hetastarch
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
HETASTARCH
-
Start Marketing Date:
1995-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Fresenius Kabi iPSUM S.r.l.
-
NDC:
66558-0212
-
Nonproprietary Name:
CEFTAZIDIME, AVIBACTAM SODIUM
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
.2; .8 kg/kg; kg/kg
-
Substance:
AVIBACTAM SODIUM; CEFTAZIDIME
-
Start Marketing Date:
2023-05-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
18124-016
-
Nonproprietary Name:
hydroxyprogesterone caproate
-
Dosage Form:
INJECTION
-
Product Type:
HUMAN PRESCRIPTION DRUG
-
Strength:
250 mg/mL
-
Substance:
HYDROXYPROGESTERONE CAPROATE
-
Start Marketing Date:
2011-02-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
66558-0197
-
Nonproprietary Name:
ICATIBANT ACETATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
ICATIBANT ACETATE
-
Start Marketing Date:
2024-01-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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