National Drug Code (NDC) Database
Kyowa Kirin Co., Ltd.
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NDC:
45793-0201
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Nonproprietary Name:
mogamulizumab
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Dosage Form:
INJECTION
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
9.5 g/L
-
Substance:
MOGAMULIZUMAB
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Start Marketing Date:
2018-08-08
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Kyowa Pharma Chemical Co., Ltd.
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NDC:
12079-2003
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Nonproprietary Name:
Istradefylline
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ISTRADEFYLLINE
-
Start Marketing Date:
2016-01-21
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
L Perrigo Company
-
NDC:
50941-957
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Nonproprietary Name:
nicotine polacrilex
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Dosage Form:
LOZENGE
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Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
4 mg/1
-
Substance:
NICOTINE
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Start Marketing Date:
2022-07-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
L. Perrigo Company
-
NDC:
50941-599
-
Nonproprietary Name:
budesonide
-
Dosage Form:
CAPSULE
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Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
3 mg/1
-
Substance:
BUDESONIDE
-
Start Marketing Date:
2025-09-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
L.N.K. International, Inc.
-
NDC:
50844-991
-
Nonproprietary Name:
Ibuprofen
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
IBUPROFEN
-
Start Marketing Date:
1988-05-24
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
La Chandra Pharmalab Private Limited
-
NDC:
83914-003
-
Nonproprietary Name:
Mifepristone
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MIFEPRISTONE
-
Start Marketing Date:
2025-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
La Crosse Milling Company
-
NDC:
72669-0555
-
Nonproprietary Name:
Colloidal Oatmeal
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
100 g/100g
-
Substance:
OATMEAL
-
Start Marketing Date:
2018-11-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Labor Zollinger AG
-
NDC:
83832-111
-
Nonproprietary Name:
RANIBIZUMAB
-
Dosage Form:
INJECTION, SOLUTION
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Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
6 mg/mL
-
Substance:
RANIBIZUMAB
-
Start Marketing Date:
2018-04-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Laboratium Ofichem BV
-
NDC:
62675-2751
-
Nonproprietary Name:
Edetate Disodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
EDETATE DISODIUM
-
Start Marketing Date:
2023-04-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Laboratoire Schmidt-Nagel
-
NDC:
73296-031
-
Nonproprietary Name:
Arnica Montana, Rhus Toxicodendron, Ledum Palustre, Calendula Officinalis, Ruta Graveolens
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
30; 6; 6; 6; 12 12kg; 12kg; 12kg; 12kg; 12kg
-
Substance:
ARNICA MONTANA; CALENDULA OFFICINALIS FLOWERING TOP; LEDUM PALUSTRE TWIG; RUTA GRAVEOLENS FLOWERING TOP; TOXICODENDRON PUBESCENS LEAF
-
Start Marketing Date:
2016-03-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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