National Drug Code (NDC) Database
Pure Peptide Pharmaceuticals Inc.
-
NDC:
87551-381
-
Nonproprietary Name:
Thymosin Alpha-1 Acetate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
THYMALFASIN
-
Start Marketing Date:
2026-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Pure Source, LLC
-
NDC:
65121-652
-
Nonproprietary Name:
Homosalate, Ethylhexyl methoxycinnamate,Butyl Methoxydibenzoylmethane, Octocrylene
-
Dosage Form:
CREAM
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
3; 10; 7.5; 2.7 g/100mL; g/100mL; g/100mL; g/100mL
-
Substance:
AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTOCRYLENE
-
Start Marketing Date:
2023-10-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
PURIFY MEDS INC
-
NDC:
87100-001
-
Nonproprietary Name:
Nicotinamide Adenine Dinucleotide (NADH) Bulk Powder, 25 kg Drum
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NICOTINAMIDE ADENINE DINUCLEOTIDE
-
Start Marketing Date:
2025-09-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Purna Pharmaceuticals NV
-
NDC:
62450-003
-
Nonproprietary Name:
vamorolone
-
Dosage Form:
SUSPENSION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
40 mg/mL
-
Substance:
VAMOROLONE
-
Start Marketing Date:
2023-11-23
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Purolite LLC
-
NDC:
68444-0005
-
Nonproprietary Name:
SODIUM POLYSTYRENE SULFONATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SODIUM POLYSTYRENE SULFONATE
-
Start Marketing Date:
2014-04-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
68166-005
-
Nonproprietary Name:
Clopidogrel Bisulfate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CLOPIDOGREL BISULFATE
-
Start Marketing Date:
2019-10-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Qilu Pharmaceutical Co. Ltd.
-
NDC:
67184-0026
-
Nonproprietary Name:
Bortezomib
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 g/25g
-
Substance:
BORTEZOMIB
-
Start Marketing Date:
2018-03-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
73548-8031
-
Nonproprietary Name:
Powdered Opium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
0.1 kg/.1kg
-
Substance:
MORPHINE
-
Start Marketing Date:
2023-12-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CII
-
Certified Through:
2026-12-31
-
NDC:
51810-052
-
Nonproprietary Name:
cefpodoxime proxetil
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CEFPODOXIME PROXETIL
-
Start Marketing Date:
2022-06-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
73212-090
-
Nonproprietary Name:
Avanafil
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
AVANAFIL
-
Start Marketing Date:
2024-03-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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