National Drug Code (NDC) Database
Sakai Chemical Industry Co.,Ltd.
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NDC:
54088-212
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Nonproprietary Name:
Zinc Oxide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
10 kg/10kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2024-12-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
SALICYLATES & CHEMICALS PRIVATE LIMITED
-
NDC:
76107-900
-
Nonproprietary Name:
ALLANTOIN
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ALLANTOIN
-
Start Marketing Date:
2012-11-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Salicylates And Chemicals Private Limited
-
NDC:
76107-251
-
Nonproprietary Name:
OCTISALATE
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
OCTISALATE
-
Start Marketing Date:
2019-09-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
SAMANTA ORGANICS PRIVATE LIMITED
-
NDC:
73281-001
-
Nonproprietary Name:
DIPHENHYDRAMINE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DIPHENHYDRAMINE HYDROCHLORIDE
-
Start Marketing Date:
2019-07-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Samsung BioLogics Co. LTD
-
NDC:
71124-0059
-
Nonproprietary Name:
adalimumab
-
Dosage Form:
INJECTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
50 mg/mL
-
Substance:
ADALIMUMAB-BWWD
-
Start Marketing Date:
2023-07-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
SAMSUNG BIOLOGICS Co., Ltd.
-
NDC:
71124-0063
-
Nonproprietary Name:
mepolizumab
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MEPOLIZUMAB
-
Start Marketing Date:
2019-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Sandoz Inc
-
NDC:
0781-3453
-
Nonproprietary Name:
BIVALIRUDIN
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
250 mg/1
-
Substance:
BIVALIRUDIN
-
Start Marketing Date:
2000-12-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Saneca Pharmaceuticals a.s.
-
NDC:
82105-006
-
Nonproprietary Name:
Nalbuphine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NALBUPHINE HYDROCHLORIDE
-
Start Marketing Date:
2026-05-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
14474-044
-
Nonproprietary Name:
Imepitoin micronized
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
5 kg/5kg
-
Substance:
IMEPITOIN
-
Start Marketing Date:
2019-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
43858-511
-
Nonproprietary Name:
Sterile Penicillin G Benzathine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
10 kg/10kg
-
Substance:
PENICILLIN G BENZATHINE
-
Start Marketing Date:
2010-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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