National Drug Code (NDC) Database
Cohance Lifsciences Limited
-
NDC:
68022-7005
-
Nonproprietary Name:
Tamsulosin Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TAMSULOSIN HYDROCHLORIDE
-
Start Marketing Date:
2016-02-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Colgate Oral Pharmaceuticals Inc.
-
NDC:
0126-0084
-
Nonproprietary Name:
Hydrogen Peroxide
-
Dosage Form:
RINSE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
15 mg/mL
-
Substance:
HYDROGEN PEROXIDE
-
Start Marketing Date:
2017-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
CONCORD BIOTECH LIMITED
-
NDC:
68254-6237
-
Nonproprietary Name:
TEMSIROLIMUS
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TEMSIROLIMUS
-
Start Marketing Date:
2011-02-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
CONCORD BIOTECH LTD
-
NDC:
68254-6234
-
Nonproprietary Name:
Everolimus
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
EVEROLIMUS
-
Start Marketing Date:
2011-08-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Contipro a.s.
-
NDC:
40004-002
-
Nonproprietary Name:
Sodium Hyaluronate type II
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
HYALURONATE SODIUM
-
Start Marketing Date:
2012-10-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Contract Pharmacal Corp.
-
NDC:
10267-5923
-
Nonproprietary Name:
Acetaminophen
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
500 mg/1
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2023-09-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Contract Pharmcal Corp.
-
NDC:
10267-5511
-
Nonproprietary Name:
Acetaminophen and Pamabrom
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
500; 25 mg/1; mg/1
-
Substance:
ACETAMINOPHEN; PAMABROM
-
Start Marketing Date:
2019-10-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
22366-088
-
Nonproprietary Name:
diluted nitroglycerin
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NITROGLYCERIN
-
Start Marketing Date:
1993-01-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Corden Pharma Bergamo S.p.A.
-
NDC:
49964-0049
-
Nonproprietary Name:
Metronidazole Benzoate Micronized
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
METRONIDAZOLE
-
Start Marketing Date:
2016-05-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
49076-7601
-
Nonproprietary Name:
Azelastine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
AZELASTINE HYDROCHLORIDE
-
Start Marketing Date:
2019-06-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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