National Drug Code (NDC) Database
Lee Pharma Ltd.
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NDC:
75945-904
-
Nonproprietary Name:
Empagliflozin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
EMPAGLIFLOZIN
-
Start Marketing Date:
2026-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Legacy Pharma USA Inc.
-
NDC:
83107-031
-
Nonproprietary Name:
paroxetine
-
Dosage Form:
CAPSULE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
7.5 mg/1
-
Substance:
PAROXETINE MESYLATE
-
Start Marketing Date:
2025-02-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Lek d.d.
-
NDC:
48866-9982
-
Nonproprietary Name:
Clavulanate Potassium diluted with Silicon Dioxide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
20 kg/20kg
-
Substance:
CLAVULANATE POTASSIUM
-
Start Marketing Date:
2022-11-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Lek Pharmaceuticals, d.d.
-
NDC:
48866-8256
-
Nonproprietary Name:
Gentamicin Sulfate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
10 kg/10kg
-
Substance:
GENTAMICIN
-
Start Marketing Date:
2013-07-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
LETCO MEDICAL, LLC
-
NDC:
62991-3246
-
Nonproprietary Name:
Ketotifen Fumarate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
KETOTIFEN FUMARATE
-
Start Marketing Date:
2026-03-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Lianhe Chemical Technology Co.,Ltd.
-
NDC:
76047-003
-
Nonproprietary Name:
Remibrutinib
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
18 kg/18kg
-
Substance:
REMIBRUTINIB
-
Start Marketing Date:
2025-09-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Lianyungang Kangle Pharmaceutical Co., Ltd.
-
NDC:
62674-001
-
Nonproprietary Name:
Acetaminophen
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2015-04-23
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Lianyungang Runzhong Pharmaceutical Co. Ltd.
-
NDC:
61662-0011
-
Nonproprietary Name:
Fulvestrant
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FULVESTRANT
-
Start Marketing Date:
2017-07-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Lianyungang Runzhong Pharmaceutical Co., Ltd.
-
NDC:
61662-0022
-
Nonproprietary Name:
Carfilzomib
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CARFILZOMIB
-
Start Marketing Date:
2023-11-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
75945-907
-
Nonproprietary Name:
Amlodipine Besylate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
AMLODIPINE BESYLATE
-
Start Marketing Date:
2026-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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