National Drug Code (NDC) Database
-
NDC:
71010-009
-
Nonproprietary Name:
TITANIUM DIOXIDE
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
85 kg/100kg
-
Substance:
TITANIUM DIOXIDE
-
Start Marketing Date:
2022-07-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Sentio BioSciences LLC
-
NDC:
49405-001
-
Nonproprietary Name:
Melarsomine Dihydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1.5 kg/1.5kg
-
Substance:
MELARSOMINE DIHYDROCHLORIDE
-
Start Marketing Date:
2017-03-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Sentio Biosciences, LLC
-
NDC:
49405-000
-
Nonproprietary Name:
PENTOSAN POLYSULFATE SODIUM
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
20 kg/20kg
-
Substance:
PENTOSAN POLYSULFATE SODIUM
-
Start Marketing Date:
2011-04-07
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
SERATEC
-
NDC:
65732-702
-
Nonproprietary Name:
Fomepizole
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FOMEPIZOLE
-
Start Marketing Date:
2008-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
SERIPHARM
-
NDC:
62422-0004
-
Nonproprietary Name:
PACLITAXEL
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
PACLITAXEL
-
Start Marketing Date:
1996-12-27
-
End Marketing Date:
2026-11-30
-
DEA Schedule:
-
Certified Through:
0000-00-00
Seripharm S.A.S.
-
NDC:
62422-0001
-
Nonproprietary Name:
PACLITAXEL
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
PACLITAXEL
-
Start Marketing Date:
2006-11-01
-
End Marketing Date:
2026-11-30
-
DEA Schedule:
-
Certified Through:
0000-00-00
Seven Star Pharmaceutical Co., Ltd.
-
NDC:
66652-2103
-
Nonproprietary Name:
Sapropterin Dihydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SAPROPTERIN DIHYDROCHLORIDE
-
Start Marketing Date:
2019-01-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Sever Pharma Solutions AB
-
NDC:
12822-0313
-
Nonproprietary Name:
SEGESTERONE ACETATE, ETHINYL ESTRADIOL
-
Dosage Form:
RING
-
Product Type:
HUMAN PRESCRIPTION DRUG
-
Strength:
17.4; 103 mg/1; mg/1
-
Substance:
ETHINYL ESTRADIOL; SEGESTERONE ACETATE
-
Start Marketing Date:
2019-08-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shaanxi Hanjiang Pharmaceutical Group Co., Ltd.
-
NDC:
63457-0022
-
Nonproprietary Name:
Fenbendazole
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FENBENDAZOLE
-
Start Marketing Date:
2018-08-07
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
SHAKTI LIFESCIENCE PRIVATE LIMITED
-
NDC:
73774-026
-
Nonproprietary Name:
TESTOSTERONE PROPIONATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TESTOSTERONE PROPIONATE
-
Start Marketing Date:
2025-02-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CIII
-
Certified Through:
2026-12-31
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