National Drug Code (NDC) Database
Premier Magnesia LLC
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NDC:
21291-2000
-
Nonproprietary Name:
Magnesium Sulfate Heptahydrate
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Dosage Form:
GRANULE
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MAGNESIUM SULFATE HEPTAHYDRATE
-
Start Marketing Date:
2022-11-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Privi Specialty Chemicals LTD.
-
NDC:
84389-000
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Nonproprietary Name:
CAMPHOR (SYNTHETIC)
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CAMPHOR (SYNTHETIC)
-
Start Marketing Date:
2024-07-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Procesadora Insuban SpA
-
NDC:
82925-001
-
Nonproprietary Name:
HEPARIN
-
Dosage Form:
BEAD
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
HEPARIN
-
Start Marketing Date:
2022-08-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
PROCOS S.p.A.
-
NDC:
46016-9522
-
Nonproprietary Name:
Chlorzoxazone
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
50 kg/50kg
-
Substance:
CHLORZOXAZONE
-
Start Marketing Date:
2016-06-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Procter & Gamble Manufacturing Company
-
NDC:
37000-999
-
Nonproprietary Name:
Eucalyptus Oil
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
EUCALYPTUS OIL
-
Start Marketing Date:
2020-10-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Prodose, Inc
-
NDC:
68210-5069
-
Nonproprietary Name:
omega-3 fish oil
-
Dosage Form:
CAPSULE
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Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
200; 1000; 300 mg/1; mg/1; mg/1
-
Substance:
DOCONEXENT; FISH OIL; ICOSAPENT
-
Start Marketing Date:
2026-01-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Prodose, Inc.
-
NDC:
68210-5070
-
Nonproprietary Name:
Acetaminophen 250mg, Aspirin 250mg and Caffeine 65mg soft gelatin capsules(Gel Tabs)
-
Dosage Form:
TABLET, COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
250; 250; 65 mg/1; mg/1; mg/1
-
Substance:
ACETAMINOPHEN; ASPIRIN; CAFFEINE
-
Start Marketing Date:
2026-05-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
12875-9998
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Nonproprietary Name:
estropipate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ESTROPIPATE
-
Start Marketing Date:
2010-11-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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