National Drug Code (NDC) Database
Kindeva Drug Delivery L.P.
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NDC:
11517-720
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Nonproprietary Name:
mometasone furoate and formoterol fumarate
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Dosage Form:
AEROSOL
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Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
5; 100 ug/1; ug/1
-
Substance:
FORMOTEROL FUMARATE; MOMETASONE FUROATE
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Start Marketing Date:
2010-06-22
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Kindeva Drug Delivery Limited
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NDC:
11517-434
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Nonproprietary Name:
Mometasone Furoate
-
Dosage Form:
AEROSOL
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Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
200 ug/1
-
Substance:
MOMETASONE FUROATE
-
Start Marketing Date:
2014-04-25
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
King Bio Inc.
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NDC:
57955-9999
-
Nonproprietary Name:
Arnica montana, Aconitum napellus, Hypericum perforatum, Ledum palustre, Magnesia phosphorica, Secale cornutum, Silicea
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Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
12; 12; 12; 12; 12; 12; 12 59mL; 59mL; 59mL; 59mL; 59mL; 59mL; 59mL
-
Substance:
ACONITUM NAPELLUS WHOLE; ARNICA MONTANA WHOLE; CLAVICEPS PURPUREA SCLEROTIUM; HYPERICUM PERFORATUM WHOLE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; RHODODENDRON TOMENTOSUM LEAFY TWIG; SILICON DIOXIDE
-
Start Marketing Date:
2025-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Kingchem Laboratories Inc.
-
NDC:
69018-110
-
Nonproprietary Name:
4-Methylpyrazole
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FOMEPIZOLE
-
Start Marketing Date:
2005-06-27
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
85378-001
-
Nonproprietary Name:
Omega-3 Acid Ethyl Esters
-
Dosage Form:
OIL
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
OMEGA-3-ACID ETHYL ESTERS
-
Start Marketing Date:
2025-04-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
51933-1100
-
Nonproprietary Name:
Potassium Chloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
POTASSIUM CHLORIDE
-
Start Marketing Date:
1980-12-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Klocke Pharma-Service GmbH
-
NDC:
87002-005
-
Nonproprietary Name:
QUETIAPINE FUMARATE
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
400 mg/1
-
Substance:
QUETIAPINE FUMARATE
-
Start Marketing Date:
2026-03-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Kolon Life Science Inc
-
NDC:
67807-148
-
Nonproprietary Name:
Zinc pyrithione
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
12 kg/25kg
-
Substance:
PYRITHIONE ZINC
-
Start Marketing Date:
2023-11-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
12294-9998
-
Nonproprietary Name:
Chlorpheniramine Maleate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CHLORPHENIRAMINE MALEATE
-
Start Marketing Date:
1978-01-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
69227-205
-
Nonproprietary Name:
Water
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
5 mL/5mL
-
Substance:
WATER
-
Start Marketing Date:
2020-10-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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