National Drug Code (NDC) Database
Hydrite Chemical Co.
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NDC:
64487-3644
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Nonproprietary Name:
BENZALKONIUM CHLORIDE Solution
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Dosage Form:
SOLUTION
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
0.1 kg/100kg
-
Substance:
BENZALKONIUM CHLORIDE
-
Start Marketing Date:
2020-08-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
ICE SpA
-
NDC:
49345-2612
-
Nonproprietary Name:
Ursodiol
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
URSODIOL
-
Start Marketing Date:
2002-05-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Icrom S.r.l.
-
NDC:
40700-0072
-
Nonproprietary Name:
BRINZOLAMIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BRINZOLAMIDE
-
Start Marketing Date:
2013-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
IMCD Switzerland AG
-
NDC:
12070-0002
-
Nonproprietary Name:
FLUOROURACIL
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FLUOROURACIL
-
Start Marketing Date:
2017-10-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Indena S.p.A
-
NDC:
17359-4200
-
Nonproprietary Name:
Thiotepa
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
THIOTEPA
-
Start Marketing Date:
2018-12-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Indena SpA
-
NDC:
17359-9100
-
Nonproprietary Name:
Docetaxel
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
DOCETAXEL ANHYDROUS
-
Start Marketing Date:
2020-03-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Indivior UK Limited
-
NDC:
71795-2200
-
Nonproprietary Name:
Buprenorphine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BUPRENORPHINE
-
Start Marketing Date:
2018-08-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CIII
-
Certified Through:
2027-12-31
-
NDC:
40700-0082
-
Nonproprietary Name:
PROCAINE HYDROCHLORIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PROCAINE HYDROCHLORIDE
-
Start Marketing Date:
2025-01-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
60152-003
-
Nonproprietary Name:
talimogene laherparepvec
-
Dosage Form:
INJECTION, SUSPENSION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100000000 [PFU]/mL
-
Substance:
TALIMOGENE LAHERPAREPVEC
-
Start Marketing Date:
2022-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
14445-026
-
Nonproprietary Name:
Rivaroxaban
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
RIVAROXABAN
-
Start Marketing Date:
2024-03-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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