National Drug Code (NDC) Database
Kaneka Eurogentec SA
-
NDC:
76356-101
-
Nonproprietary Name:
GLUCARPIDASE
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1000 U/mL
-
Substance:
GLUCARPIDASE
-
Start Marketing Date:
2015-11-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
KAO USA
-
NDC:
10596-194
-
Nonproprietary Name:
Octocrylene Ethylhexyl Salicylate Homosalate Butyl Methoxydibenzoylmethane
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
3.5; 11.7; 5.9; 5.9 kg/100kg; kg/100kg; kg/100kg; kg/100kg
-
Substance:
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
-
Start Marketing Date:
2022-12-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Kekule Life Sciences Limited
-
NDC:
87358-125
-
Nonproprietary Name:
Lapatinib Ditosylate Monohydrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LAPATINIB DITOSYLATE
-
Start Marketing Date:
2026-06-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Kellin Chemicals (Zhangjiagang) Co., Ltd.
-
NDC:
81089-000
-
Nonproprietary Name:
ISOPROPYL ALCOHOL
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ISOPROPYL ALCOHOL
-
Start Marketing Date:
2020-11-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
KENTEGRA PYRETHRUM COMPANY LIMITED
-
NDC:
83172-100
-
Nonproprietary Name:
Pyrethrum Extract
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
50 kg/100kg
-
Substance:
PYRETHRUM EXTRACT
-
Start Marketing Date:
2022-12-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Kenvue Brands LLC
-
NDC:
50580-589
-
Nonproprietary Name:
acetaminophen
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
500 mg/1
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2019-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Kenvue Canada Inc.
-
NDC:
65498-792
-
Nonproprietary Name:
Cetirizine Hydrochloride
-
Dosage Form:
TABLET, CHEWABLE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
5 mg/1
-
Substance:
CETIRIZINE HYDROCHLORIDE
-
Start Marketing Date:
2022-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Keshava Organics Pvt Ltd
-
NDC:
63943-4683
-
Nonproprietary Name:
Dexchlorpheniramine Maleate
-
Dosage Form:
CONCENTRATE
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DEXCHLORPHENIRAMINE MALEATE
-
Start Marketing Date:
2000-10-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
17349-0022
-
Nonproprietary Name:
SULFACETAMIDE SODIUM
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
50 kg/50kg
-
Substance:
SULFACETAMIDE SODIUM
-
Start Marketing Date:
1984-06-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
53220-123
-
Nonproprietary Name:
Nilutamide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NILUTAMIDE
-
Start Marketing Date:
2016-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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