National Drug Code (NDC) Database
Optimus Drugs Private Limited
-
NDC:
59285-043
-
Nonproprietary Name:
MIDODRINE HYDROCHLORIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MIDODRINE HYDROCHLORIDE
-
Start Marketing Date:
2021-12-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Orchev Pharma Private Limited
-
NDC:
70910-0002
-
Nonproprietary Name:
Famotidine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FAMOTIDINE
-
Start Marketing Date:
2022-06-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Organo Sintesis, S.A. de C.V.
-
NDC:
51606-004
-
Nonproprietary Name:
Benzalkonium Chloride
-
Dosage Form:
SOLUTION, CONCENTRATE
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BENZALKONIUM CHLORIDE
-
Start Marketing Date:
2024-11-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Organon Heist
-
NDC:
52408-0130
-
Nonproprietary Name:
desloratadine
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
5 mg/1
-
Substance:
DESLORATADINE
-
Start Marketing Date:
2022-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
ORGANON PHARMA (UK) LIMITED
-
NDC:
60312-0960
-
Nonproprietary Name:
losartan potassium
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100 mg/1
-
Substance:
LOSARTAN POTASSIUM
-
Start Marketing Date:
1995-04-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Oriental Aromatics Limited
-
NDC:
59599-120
-
Nonproprietary Name:
Camphor
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CAMPHOR (SYNTHETIC)
-
Start Marketing Date:
2018-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Orion Corporation, ORION PHARMA
-
NDC:
52483-6300
-
Nonproprietary Name:
darolutamide
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
300 mg/1
-
Substance:
DAROLUTAMIDE
-
Start Marketing Date:
2019-12-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
63785-115
-
Nonproprietary Name:
Ceftiofur Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
10 kg/10kg
-
Substance:
CEFTIOFUR HYDROCHLORIDE
-
Start Marketing Date:
2014-04-23
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
75852-816
-
Nonproprietary Name:
ivabradine hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
IVABRADINE HYDROCHLORIDE
-
Start Marketing Date:
2014-02-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
83030-377
-
Nonproprietary Name:
Physostigmine Salicylate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
100 g/100g
-
Substance:
PHYSOSTIGMINE SALICYLATE
-
Start Marketing Date:
2022-10-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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