National Drug Code (NDC) Database
Gilead Sciences, Inc.
-
NDC:
24525-0025
-
Nonproprietary Name:
AZTREONAM
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
AZTREONAM
-
Start Marketing Date:
2015-12-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Glacial Grain Spirits, LLC
-
NDC:
80946-3739
-
Nonproprietary Name:
190 Proof Specially Denatured Alcohol (SDA) 40B
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100 L/100L
-
Substance:
ALCOHOL
-
Start Marketing Date:
2003-12-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Glaxo Operations UK Ltd
-
NDC:
63379-119
-
Nonproprietary Name:
Linerixibat
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
40 mg/1
-
Substance:
LINERIXIBAT
-
Start Marketing Date:
2026-03-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Glaxo Wellcome Manufacturing Pte. Ltd
-
NDC:
52482-020
-
Nonproprietary Name:
Daprodustat
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DAPRODUSTAT
-
Start Marketing Date:
2023-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Global Calcium Private Limited
-
NDC:
64162-0448
-
Nonproprietary Name:
Calcium Gluconate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CALCIUM GLUCONATE MONOHYDRATE
-
Start Marketing Date:
2017-01-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Global Calcium Private Limited Unit III
-
NDC:
64162-3448
-
Nonproprietary Name:
Calcium Gluconate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CALCIUM GLUCONATE MONOHYDRATE
-
Start Marketing Date:
2025-07-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Globela Pharma Pvt Ltd
-
NDC:
85177-005
-
Nonproprietary Name:
Guaifenesin 400mg
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
400 mg/1
-
Substance:
GUAIFENESIN
-
Start Marketing Date:
2025-07-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Glochem Industries Limited
-
NDC:
24234-0007
-
Nonproprietary Name:
TELMISARTAN
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TELMISARTAN
-
Start Marketing Date:
2026-03-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
68083-477
-
Nonproprietary Name:
olopatadine hydrochloride ophthalmic
-
Dosage Form:
SOLUTION/ DROPS
-
Product Type:
BULK INGREDIENT
-
Strength:
1 mg/mL
-
Substance:
OLOPATADINE HYDROCHLORIDE
-
Start Marketing Date:
2020-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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