National Drug Code (NDC) Database
Clariant Chemicals (Huizhou) Ltd
-
NDC:
71932-100
-
Nonproprietary Name:
POLYETHYLENE GLYCOL 3350
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
POLYETHYLENE GLYCOL 3350
-
Start Marketing Date:
2021-11-04
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Clariant Produkte (deutschland) Gmbh
-
NDC:
43421-300
-
Nonproprietary Name:
POLYETHYLENE GLYCOL 3350
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
POLYETHYLENE GLYCOL 3350
-
Start Marketing Date:
2026-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
76278-1120
-
Nonproprietary Name:
DROXIDOPA
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DROXIDOPA
-
Start Marketing Date:
2016-11-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Clarochem Ireland Ltd.
-
NDC:
76278-1700
-
Nonproprietary Name:
fosfomycin trometamol
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FOSFOMYCIN TROMETHAMINE
-
Start Marketing Date:
2025-03-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
CLINIQUE LABORATORIES LLC
-
NDC:
49527-910
-
Nonproprietary Name:
avobenzone,homosalate,octisalate,octocrylene
-
Dosage Form:
CREAM
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
30; 70; 45; 50 g/kg; g/kg; g/kg; g/kg
-
Substance:
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
-
Start Marketing Date:
2025-05-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
51434-1330
-
Nonproprietary Name:
Tacrolimus
-
Dosage Form:
GRANULE, FOR SUSPENSION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 mg/1
-
Substance:
TACROLIMUS
-
Start Marketing Date:
2018-05-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Coating Place, LLC
-
NDC:
81842-749
-
Nonproprietary Name:
Methylphenidate HCl
-
Dosage Form:
CAPSULE, EXTENDED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
20 mg/1
-
Substance:
METHYLPHENIDATE
-
Start Marketing Date:
2019-05-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CII
-
Certified Through:
2027-12-31
Cohance Lifescience Limited
-
NDC:
68022-7015
-
Nonproprietary Name:
Entacapone
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ENTACAPONE
-
Start Marketing Date:
2016-02-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Cohance Lifesciences Limited
-
NDC:
76072-1020
-
Nonproprietary Name:
Buspirone Hydrochloride (BPN)
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BUSPIRONE HYDROCHLORIDE
-
Start Marketing Date:
2025-01-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Cohance Lifescienes Limited
-
NDC:
68022-7002
-
Nonproprietary Name:
Fenoprofen Calcium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FENOPROFEN CALCIUM
-
Start Marketing Date:
2016-02-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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