National Drug Code (NDC) Database
HOVIONE LIMITED
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NDC:
51473-1906
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Nonproprietary Name:
Suzetrigine SDD
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Dosage Form:
POWDER
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
25 kg/100kg
-
Substance:
SUZETRIGINE
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Start Marketing Date:
2025-01-30
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2027-12-31
HOVIONE LLC
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NDC:
42052-2001
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Nonproprietary Name:
Elexacaftor Tezacaftor Ivacaftor
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Dosage Form:
TABLET, COATED
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Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100; 75; 50 mg/1; mg/1; mg/1
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Substance:
ELEXACAFTOR; IVACAFTOR; TEZACAFTOR
-
Start Marketing Date:
2019-10-21
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Huanggang Saikang Pharmaceutical Co., Ltd.
-
NDC:
87171-001
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Nonproprietary Name:
melatonin
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
MELATONIN
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Start Marketing Date:
2025-10-20
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
58135-001
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Nonproprietary Name:
OMEGA-3-ACID ETHYL ESTERS
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Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
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Strength:
190 kg/190kg
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Substance:
OMEGA-3-ACID ETHYL ESTERS
-
Start Marketing Date:
2013-04-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Huatai Pharma Inc.
-
NDC:
79568-000
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Nonproprietary Name:
ICOSAPENT ETHYL
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ICOSAPENT ETHYL
-
Start Marketing Date:
2020-06-26
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hubei Chengtian Pharmaceutical Co., Ltd.
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NDC:
82758-505
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Nonproprietary Name:
NINTEDANIB ESYLATE
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NINTEDANIB ESYLATE
-
Start Marketing Date:
2022-05-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hubei Enoray Biopharmaceutical Co., Ltd.
-
NDC:
70398-0003
-
Nonproprietary Name:
Enoxaparin Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ENOXAPARIN SODIUM
-
Start Marketing Date:
2017-10-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hubei Gedian humanwell Pharmaceutical Co., Ltd
-
NDC:
51508-213
-
Nonproprietary Name:
EPLERENONE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
EPLERENONE
-
Start Marketing Date:
2026-04-23
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Hubei Gedian Humanwell Pharmaceutical Co., Ltd.
-
NDC:
51508-212
-
Nonproprietary Name:
Medroxyprogesterone acetate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MEDROXYPROGESTERONE ACETATE
-
Start Marketing Date:
2026-03-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
51035-003
-
Nonproprietary Name:
SODIUM HYALURONATE
-
Dosage Form:
SOLUTION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
SODIUM HYALURONATE
-
Start Marketing Date:
2025-02-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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