National Drug Code (NDC) Database
MannKind Corporation
-
NDC:
47918-191
-
Nonproprietary Name:
INSULIN HUMAN
-
Dosage Form:
POWDER, METERED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
12 [arb'U]/1
-
Substance:
INSULIN HUMAN
-
Start Marketing Date:
2026-01-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
57741-4100
-
Nonproprietary Name:
Cariprazine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CARIPRAZINE
-
Start Marketing Date:
2024-09-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Marcus Research Laboratory, Inc.
-
NDC:
44242-100
-
Nonproprietary Name:
POVIDONE-IODINE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
POVIDONE-IODINE
-
Start Marketing Date:
1981-04-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Mariager Salt Specialties A/S
-
NDC:
82056-0001
-
Nonproprietary Name:
Sodium Chloride
-
Dosage Form:
CRYSTAL
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SODIUM CHLORIDE
-
Start Marketing Date:
2021-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Matrix Pharmacorp Private Limited
-
NDC:
84206-0116
-
Nonproprietary Name:
Sertraline Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
10 kg/10kg
-
Substance:
SERTRALINE HYDROCHLORIDE
-
Start Marketing Date:
2025-10-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
50546-858
-
Nonproprietary Name:
Carbidopa and Levodopa
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
25; 250 mg/1; mg/1
-
Substance:
CARBIDOPA; LEVODOPA
-
Start Marketing Date:
2018-03-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Mayne Pharma International Pty Ltd.
-
NDC:
50546-560
-
Nonproprietary Name:
doxycycline hyclate
-
Dosage Form:
TABLET, DELAYED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
60 mg/1
-
Substance:
DOXYCYCLINE HYCLATE
-
Start Marketing Date:
2022-06-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Mazza Healthcare, LLC
-
NDC:
81280-004
-
Nonproprietary Name:
Povidone-Iodine
-
Dosage Form:
SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.1 mg/mL
-
Substance:
POVIDONE-IODINE
-
Start Marketing Date:
2024-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
McKinley Resources Inc.
-
NDC:
86014-205
-
Nonproprietary Name:
MICONAZOLE NITRATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MICONAZOLE NITRATE
-
Start Marketing Date:
2019-06-07
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
McLaughlin Gormley King Company
-
NDC:
55464-101
-
Nonproprietary Name:
Pyrethrum Extract and Piperonyl Butoxide
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
.194; .016 g/kg; g/kg
-
Substance:
PIPERONYL BUTOXIDE; PYRETHRUM EXTRACT
-
Start Marketing Date:
2019-01-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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