National Drug Code (NDC) Database
Elanco US Inc.
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NDC:
58198-8291
-
Nonproprietary Name:
lotilaner, moxidectin, praziquantel, and pyrantel
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Dosage Form:
TABLET, CHEWABLE
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
900; .9; 228; 228 mg/1; mg/1; mg/1; mg/1
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Substance:
LOTILANER; MOXIDECTIN; PRAZIQUANTEL; PYRANTEL PAMOATE
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Start Marketing Date:
2024-10-07
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Elementis SRL, INC
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NDC:
72450-771
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Nonproprietary Name:
Aluminum Zirconium Tetrachlorohydrex Gly
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Dosage Form:
SOLUTION
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
0.34 kg/kg
-
Substance:
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
-
Start Marketing Date:
2021-03-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Elementis SRL, Inc.
-
NDC:
72450-997
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Nonproprietary Name:
Aluminum Zirconium Pentachlorohydrex Gly
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY
-
Start Marketing Date:
2025-06-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Eli Lilly and Company
-
NDC:
0110-3977
-
Nonproprietary Name:
selpercatinib
-
Dosage Form:
CAPSULE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
40 mg/1
-
Substance:
SELPERCATINIB
-
Start Marketing Date:
2021-04-01
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Eli Lilly Italia SPA
-
NDC:
54568-837
-
Nonproprietary Name:
tirzepatide
-
Dosage Form:
INJECTION, SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
7.5 mg/.5mL
-
Substance:
TIRZEPATIDE
-
Start Marketing Date:
2023-07-13
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Eli Lilly Kinsale Limited
-
NDC:
63419-0874
-
Nonproprietary Name:
Donanemab
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DONANEMAB
-
Start Marketing Date:
2022-03-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
ELITE ADVANCED MATERIALS SDN. BHD.
-
NDC:
83475-001
-
Nonproprietary Name:
Isopropyl Alcohol
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
99 L/100L
-
Substance:
ISOPROPYL ALCOHOL
-
Start Marketing Date:
2023-05-26
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
14803-151
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Nonproprietary Name:
acetaminophenand caffeine
-
Dosage Form:
TABLET
-
Product Type:
HUMAN OTC DRUG
-
Strength:
500; 65 mg/1; mg/1
-
Substance:
ACETAMINOPHEN; CAFFEINE
-
Start Marketing Date:
2024-03-07
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Elysium Pharmaceuticals Limited
-
NDC:
14803-912
-
Nonproprietary Name:
Diphenhydramine Hydrochloride 25
-
Dosage Form:
CAPSULE
-
Product Type:
HUMAN OTC DRUG
-
Strength:
25 mg/1
-
Substance:
DIPHENHYDRAMINE HYDROCHLORIDE
-
Start Marketing Date:
2025-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
55603-805
-
Nonproprietary Name:
Sucralfate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SUCRALFATE
-
Start Marketing Date:
2013-11-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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