National Drug Code (NDC) Database
Kothari Phytochemicals International
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NDC:
52537-004
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Nonproprietary Name:
CHLORPROPAMIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CHLORPROPAMIDE
-
Start Marketing Date:
2015-06-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Kowon International Korea Co.ltd
-
NDC:
73493-050
-
Nonproprietary Name:
Titanium Dioxide
-
Dosage Form:
LIQUID
-
Product Type:
HUMAN OTC DRUG
-
Strength:
5 kg/20kg
-
Substance:
TITANIUM DIOXIDE
-
Start Marketing Date:
2019-11-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Kreative Organics Private Limited
-
NDC:
58793-010
-
Nonproprietary Name:
Etodolac
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ETODOLAC
-
Start Marketing Date:
2016-12-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
KusuMa PharMa
-
NDC:
70629-7000
-
Nonproprietary Name:
Potassium Nitrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
POTASSIUM NITRATE
-
Start Marketing Date:
2016-04-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Kyorin Pharmaceutical Group Facility Co., Ltd.
-
NDC:
53476-1155
-
Nonproprietary Name:
GATIFLOXACIN
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GATIFLOXACIN
-
Start Marketing Date:
2018-07-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
KYOWA HAKKO BIO CO., LTD.
-
NDC:
12497-1054
-
Nonproprietary Name:
L-Glutathione oxidized
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
GLUTATHIONE
-
Start Marketing Date:
1988-12-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
83221-008
-
Nonproprietary Name:
Ferric Carboxymaltose
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FERRIC CARBOXYMALTOSE
-
Start Marketing Date:
2025-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
82364-137
-
Nonproprietary Name:
Guaifenesin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GUAIFENESIN
-
Start Marketing Date:
2024-04-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
63934-110
-
Nonproprietary Name:
Triclosan
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TRICLOSAN
-
Start Marketing Date:
2000-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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