National Drug Code (NDC) Database
Otsuka Chemical Co., Ltd.
-
NDC:
60212-352
-
Nonproprietary Name:
TAZOBACTAM
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TAZOBACTAM
-
Start Marketing Date:
1993-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
OTSUKA PHARMACEUTICAL CO. LTD.
-
NDC:
46602-0001
-
Nonproprietary Name:
brexpiprazole
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BREXPIPRAZOLE
-
Start Marketing Date:
2015-07-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
OTSUKA PHARMACEUTICAL CO., LTD.
-
NDC:
46602-1034
-
Nonproprietary Name:
ARIPIPRAZOLE
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
30 mg/1
-
Substance:
ARIPIPRAZOLE
-
Start Marketing Date:
2016-04-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Oy Chembiz Ab Ltd
-
NDC:
81652-110
-
Nonproprietary Name:
Zinc oxide dispersion
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
30 kg/50kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2021-03-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Oy West eSales Ab Ltd
-
NDC:
82464-001
-
Nonproprietary Name:
OATMEAL
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
OATMEAL
-
Start Marketing Date:
2022-01-04
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
P & L Development, LLC
-
NDC:
59726-613
-
Nonproprietary Name:
Nicotine Polacrilex
-
Dosage Form:
GUM, CHEWING
-
Product Type:
BULK INGREDIENT
-
Strength:
4 mg/1
-
Substance:
NICOTINE
-
Start Marketing Date:
2024-10-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Package Kare Inc., D.B.A. Advanced Powder Solutions
-
NDC:
80933-004
-
Nonproprietary Name:
Zinc Oxide
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
94 kg/100kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2020-07-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Padagis Israel Pharmaceuticals Ltd
-
NDC:
67438-045
-
Nonproprietary Name:
triamcinolone acetonide
-
Dosage Form:
SPRAY, METERED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
55 ug/1
-
Substance:
TRIAMCINOLONE ACETONIDE
-
Start Marketing Date:
2015-06-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
PADARSH PHARMACEUTICALS PVT. LTD
-
NDC:
59134-002
-
Nonproprietary Name:
MAGNESIUM HYDROXIDE
-
Dosage Form:
PASTE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.3 kg/.3kg
-
Substance:
MAGNESIUM HYDROXIDE
-
Start Marketing Date:
2024-04-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
70054-036
-
Nonproprietary Name:
Bismuth Subcitrate Potassium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
16 kg/16kg
-
Substance:
BISMUTH SUBCITRATE POTASSIUM
-
Start Marketing Date:
2023-03-07
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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