National Drug Code (NDC) Database
Hikma Pharmaceuticals LLC
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NDC:
59115-823
-
Nonproprietary Name:
Fluticasone propionate ,USP (Micronized)
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FLUTICASONE PROPIONATE
-
Start Marketing Date:
2018-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hiray Pharma Solutions Ltd.
-
NDC:
85203-000
-
Nonproprietary Name:
Salcaprozate Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SALCAPROZATE SODIUM
-
Start Marketing Date:
2026-04-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Hisun Pharmaceutical (Hangzhou) Co., Ltd.
-
NDC:
51187-0010
-
Nonproprietary Name:
Sirolimus
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SIROLIMUS
-
Start Marketing Date:
2019-09-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hisun Pharmaceutical (Nantong) Co., Ltd.
-
NDC:
69011-0008
-
Nonproprietary Name:
Fluralaner
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FLURALANER
-
Start Marketing Date:
2025-04-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
HK Kolmar Canada, Inc
-
NDC:
49354-167
-
Nonproprietary Name:
ZINC OXIDE
-
Dosage Form:
LOTION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2024-07-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Holiday Labs Mexico, S.A. De C.V.
-
NDC:
52286-5500
-
Nonproprietary Name:
Albendazole
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ALBENDAZOLE
-
Start Marketing Date:
2009-09-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Holland Company, Inc.
-
NDC:
51378-961
-
Nonproprietary Name:
Aluminum sulfate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
ALUMINUM SULFATE
-
Start Marketing Date:
1983-09-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Honeywell Specialty Chemicals Seelze GmbH
-
NDC:
42402-101
-
Nonproprietary Name:
stannous fluoride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
STANNOUS FLUORIDE
-
Start Marketing Date:
2012-10-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
59115-809
-
Nonproprietary Name:
Glycopyrrolate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GLYCOPYRROLATE
-
Start Marketing Date:
2011-09-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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