National Drug Code (NDC) Database
Ubrogepant
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NDC:
69766-109
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Nonproprietary Name:
ubrogepant
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
UBROGEPANT
-
Start Marketing Date:
2023-08-22
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
UCB Farchim S.A.
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NDC:
28877-5970
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Nonproprietary Name:
levetiracetam
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Dosage Form:
TABLET, FILM COATED
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
1000 mg/1
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Substance:
LEVETIRACETAM
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Start Marketing Date:
2000-04-24
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
UCB Pharma S.A.
-
NDC:
36998-6000
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Nonproprietary Name:
bimekizumab
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Dosage Form:
INJECTION, SOLUTION
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
160 mg/mL
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Substance:
BIMEKIZUMAB
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Start Marketing Date:
2023-10-17
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
UCB Pharma SA
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NDC:
36998-9550
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Nonproprietary Name:
cetirizine hydrochloride and pseudoephedrine hydrochloride
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Dosage Form:
TABLET, EXTENDED RELEASE
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
5; 120 mg/1; mg/1
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Substance:
CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
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Start Marketing Date:
2001-08-10
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Umicore Agrentina s.A.
-
NDC:
72659-863
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Nonproprietary Name:
Carboplatin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
CARBOPLATIN
-
Start Marketing Date:
2017-01-02
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Unilab Chemicals and Pharmaceuticals Private Limited
-
NDC:
25119-7000
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Nonproprietary Name:
CHLOROXYLENOL
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
CHLOROXYLENOL
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Start Marketing Date:
2023-10-20
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Unilab Pharmaceuticals and Chemicals Private Limited
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NDC:
25119-8000
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Nonproprietary Name:
Guaifenesin 95% DC
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Dosage Form:
GRANULE
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Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GUAIFENESIN
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Start Marketing Date:
2025-10-01
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
28877-7300
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Nonproprietary Name:
certolizumab pegol
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Dosage Form:
INJECTION, SOLUTION
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Product Type:
BULK INGREDIENT
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Strength:
1 g/g
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Substance:
CERTOLIZUMAB PEGOL
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Start Marketing Date:
2017-12-07
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
53747-106
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Nonproprietary Name:
allopurinol
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ALLOPURINOL
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Start Marketing Date:
2025-11-13
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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