National Drug Code (NDC) Database
Village Pharma LLC
-
NDC:
71574-124
-
Nonproprietary Name:
LIDOCAINE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LIDOCAINE HYDROCHLORIDE
-
Start Marketing Date:
2022-05-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Village Pharma, LLC
-
NDC:
71574-120
-
Nonproprietary Name:
GABAPENTIN, KETOPROFEN AND LIDOCAINE
-
Dosage Form:
KIT
-
Product Type:
BULK INGREDIENT
-
Strength:
-
Substance:
-
Start Marketing Date:
2022-10-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Viloxazine Hydrochloride
-
NDC:
70966-0044
-
Nonproprietary Name:
Viloxazine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
VILOXAZINE HYDROCHLORIDE
-
Start Marketing Date:
2021-04-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Virchow Labs
-
NDC:
66249-0456
-
Nonproprietary Name:
Sulfamethoxazole
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SULFAMETHOXAZOLE
-
Start Marketing Date:
1984-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Virtu Pharmako (Zhejiang) Co., Ltd.
-
NDC:
85827-302
-
Nonproprietary Name:
semaglutide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
SEMAGLUTIDE
-
Start Marketing Date:
2025-12-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
VistaPharm, LLC
-
NDC:
66689-681
-
Nonproprietary Name:
Methadone Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
METHADONE HYDROCHLORIDE
-
Start Marketing Date:
2009-10-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CII
-
Certified Through:
2026-12-31
-
NDC:
70159-008
-
Nonproprietary Name:
Hydroxyzine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
HYDROXYZINE DIHYDROCHLORIDE
-
Start Marketing Date:
2022-12-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
51686-0015
-
Nonproprietary Name:
Ranolazine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
RANOLAZINE
-
Start Marketing Date:
2025-12-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
32995-5422
-
Nonproprietary Name:
metformin hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
METFORMIN HYDROCHLORIDE
-
Start Marketing Date:
2006-02-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
42337-410
-
Nonproprietary Name:
Efinaconazole
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
EFINACONAZOLE
-
Start Marketing Date:
2026-06-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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