National Drug Code (NDC) Database
Früeh Verpackungstechnik AG
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NDC:
71082-210
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Nonproprietary Name:
furosemide injection 80 mg/ 10 mL
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Dosage Form:
INJECTION
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
8 mg/mL
-
Substance:
FUROSEMIDE
-
Start Marketing Date:
2022-11-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Fujian Disheng Technology Co., Ltd.
-
NDC:
83801-0000
-
Nonproprietary Name:
OCTOCRYLENE
-
Dosage Form:
LIQUID
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Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
OCTOCRYLENE
-
Start Marketing Date:
2023-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
67630-0016
-
Nonproprietary Name:
Nystatin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NYSTATIN
-
Start Marketing Date:
2026-02-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Fujian Genohope Biotech Ltd.
-
NDC:
84502-113
-
Nonproprietary Name:
Semaglutide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
SEMAGLUTIDE
-
Start Marketing Date:
2026-05-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Fujian Kerui Pharmaceutical Co., Ltd.
-
NDC:
59573-0004
-
Nonproprietary Name:
Sirolimus
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
500 g/500g
-
Substance:
SIROLIMUS
-
Start Marketing Date:
2017-12-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Fujian Nanping Green Pine Chemical Co., Ltd.
-
NDC:
52330-002
-
Nonproprietary Name:
CAMPHOR (SYNTHETIC)
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CAMPHOR (SYNTHETIC)
-
Start Marketing Date:
2021-11-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Fujian South Pharmaceutical Co. Ltd.
-
NDC:
52222-0001
-
Nonproprietary Name:
Paclitaxel
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
PACLITAXEL
-
Start Marketing Date:
2018-12-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Fujian South Pharmaceutical Co., Ltd.
-
NDC:
52222-0003
-
Nonproprietary Name:
docetaxel trihydrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
DOCETAXEL
-
Start Marketing Date:
2025-07-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
FUJIFILM Diosynth Biotechnologies UK Ltd.
-
NDC:
63508-007
-
Nonproprietary Name:
denileukin diftitox
-
Dosage Form:
INJECTION, SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
150 ug/mL
-
Substance:
DENILEUKIN DIFTITOX-CXDL
-
Start Marketing Date:
2025-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
FUJIMOTO CHEMICALS CO., LTD.
-
NDC:
10261-2123
-
Nonproprietary Name:
ALECTINIB HYDROCHLORIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
ALECTINIB HYDROCHLORIDE
-
Start Marketing Date:
2017-11-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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