National Drug Code (NDC) Database
RioCare India Private Limited
-
NDC:
44331-7301
-
Nonproprietary Name:
Simethicone Emulsion
-
Dosage Form:
EMULSION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DIMETHICONE
-
Start Marketing Date:
2008-09-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Riocare India Pvt Ltd
-
NDC:
44331-5001
-
Nonproprietary Name:
Simethicone 50% Powder
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DIMETHICONE
-
Start Marketing Date:
2017-10-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
RMC Performance Chemicals Private Limited
-
NDC:
87285-1000
-
Nonproprietary Name:
Aspirin / Acetylsalicylic Acid
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ACETYLSALICYLIC ACID
-
Start Marketing Date:
2026-02-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Roche Carolina Inc.
-
NDC:
63482-099
-
Nonproprietary Name:
capecitabine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CAPECITABINE
-
Start Marketing Date:
1998-04-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Roerig
-
NDC:
0049-1582
-
Nonproprietary Name:
glipizide
-
Dosage Form:
TABLET, EXTENDED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
10 mg/1
-
Substance:
GLIPIZIDE
-
Start Marketing Date:
2013-05-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Rolabo Outsourcing S.L.
-
NDC:
63827-1018
-
Nonproprietary Name:
Deutetrabenazine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DEUTETRABENAZINE
-
Start Marketing Date:
2025-04-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
63827-1015
-
Nonproprietary Name:
ATROPINE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ATROPINE
-
Start Marketing Date:
2014-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
49629-046
-
Nonproprietary Name:
Acoramidis hydrochloride
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
356 mg/1
-
Substance:
ACORAMIDIS HYDROCHLORIDE
-
Start Marketing Date:
2024-11-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
61704-001
-
Nonproprietary Name:
MANNOSE TRIFLATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 mg/mg
-
Substance:
.BETA.-D-MANNOPYRANOSE 1,3,4,6-TETRA-O-ACETATE 2-O-TRIFLUOROMETHANESULFONATE
-
Start Marketing Date:
2014-01-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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