National Drug Code (NDC) Database
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NDC:
58624-0713
-
Nonproprietary Name:
Theophylline Anhydrous
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
THEOPHYLLINE
-
Start Marketing Date:
2026-01-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
50915-118
-
Nonproprietary Name:
Piperacillin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
60 kg/60kg
-
Substance:
PIPERACILLIN
-
Start Marketing Date:
2010-06-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shandong Topscience Biotech Co., Ltd.
-
NDC:
84109-001
-
Nonproprietary Name:
Sodium Hyaluronate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
HYALURONATE SODIUM
-
Start Marketing Date:
2023-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shandong Xinhua Pharmaceutical Co Ltd.
-
NDC:
58624-7006
-
Nonproprietary Name:
Ibuprofen
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
200 mg/1
-
Substance:
IBUPROFEN
-
Start Marketing Date:
2021-06-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shandong Xinhua Pharmaceutical Co. Ltd
-
NDC:
58624-0620
-
Nonproprietary Name:
Antipyrine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ANTIPYRINE
-
Start Marketing Date:
2008-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shandong Xinhua Pharmaceutical Co., Ltd.
-
NDC:
58624-6004
-
Nonproprietary Name:
ibuprofen
-
Dosage Form:
TABLET, COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
300 mg/1
-
Substance:
IBUPROFEN
-
Start Marketing Date:
2025-02-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shandong Xinhua Pharmaceutical Company Linited
-
NDC:
58624-0411
-
Nonproprietary Name:
Ethyl Icosapentate
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ICOSAPENT ETHYL
-
Start Marketing Date:
2021-05-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Shanghai Ajinomoto Amino Acid Co.,Ltd.
-
NDC:
72013-930
-
Nonproprietary Name:
L-Threonine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
THREONINE
-
Start Marketing Date:
2017-01-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shanghai Ambiopharm, Inc
-
NDC:
41524-0012
-
Nonproprietary Name:
Semaglutide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
SEMAGLUTIDE
-
Start Marketing Date:
2021-12-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
71783-001
-
Nonproprietary Name:
Tiamulin fumarate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TIAMULIN FUMARATE
-
Start Marketing Date:
2018-05-23
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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