National Drug Code (NDC) Database
Cosmos Personal Care (Malaysia) SDN. BHD.
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NDC:
85704-004
-
Nonproprietary Name:
OCTISALATE
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
OCTISALATE
-
Start Marketing Date:
2025-12-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
61788-5000
-
Nonproprietary Name:
Cefpodoxime Proxetil
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CEFPODOXIME PROXETIL
-
Start Marketing Date:
2004-05-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Croda Europe
-
NDC:
58013-1051
-
Nonproprietary Name:
Titanium Dioxide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TITANIUM DIOXIDE
-
Start Marketing Date:
2020-02-04
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Croda Europe Ltd
-
NDC:
76073-0100
-
Nonproprietary Name:
Fish oil
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
OMEGA-3-ACID ETHYL ESTERS
-
Start Marketing Date:
2011-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Croda Europe Ltd.
-
NDC:
76073-0200
-
Nonproprietary Name:
Titanium Dioxide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TITANIUM DIOXIDE
-
Start Marketing Date:
2017-08-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
CSPC Weisheng Pharmaceutical (Shijiazhuang) Co., Ltd
-
NDC:
72783-1002
-
Nonproprietary Name:
Sodium Ascorbate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SODIUM ASCORBATE
-
Start Marketing Date:
2020-04-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.
-
NDC:
52962-630
-
Nonproprietary Name:
Penicillin G Procaine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PENICILLIN G PROCAINE
-
Start Marketing Date:
2024-08-01
-
End Marketing Date:
2035-07-01
-
DEA Schedule:
-
Certified Through:
0000-00-00
CTX Lifesciences Pvt. Ltd.
-
NDC:
42419-038
-
Nonproprietary Name:
Linagliptin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
LINAGLIPTIN
-
Start Marketing Date:
2025-11-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
CU Chemie Uetikon GmbH
-
NDC:
54382-124
-
Nonproprietary Name:
SODIUM PHENYLACETATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SODIUM PHENYLACETATE
-
Start Marketing Date:
2002-09-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
CU Chemie Uetikon GmbH (340717289)
-
NDC:
54382-128
-
Nonproprietary Name:
KETAMINE HYDROCHLORIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
KETAMINE HYDROCHLORIDE
-
Start Marketing Date:
1989-08-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CIII
-
Certified Through:
2026-12-31
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