National Drug Code (NDC) Database
Viyash Life Sciences Private Limited
-
NDC:
82245-0220
-
Nonproprietary Name:
Nilotinib Premix
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NILOTINIB HYDROCHLORIDE MONOHYDRATE
-
Start Marketing Date:
2026-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Vovantis Laboratories Private Limited
-
NDC:
51114-0924
-
Nonproprietary Name:
Pyrantel Pamoate
-
Dosage Form:
GRANULE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
720.5 mg/.0015kg
-
Substance:
PYRANTEL PAMOATE
-
Start Marketing Date:
2024-09-23
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Voyant Beauty, Inc.
-
NDC:
61047-157
-
Nonproprietary Name:
avobenzone,homosalate, octisalate, octocrylene
-
Dosage Form:
LOTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
3; 10; 5; 5 kg/100kg; kg/100kg; kg/100kg; kg/100kg
-
Substance:
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
-
Start Marketing Date:
2026-03-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
53734-336
-
Nonproprietary Name:
Nystatin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NYSTATIN
-
Start Marketing Date:
2017-08-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
W. R. Grace & C0.-Conn.
-
NDC:
22568-1093
-
Nonproprietary Name:
Flurbiprofen
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FLURBIPROFEN
-
Start Marketing Date:
2006-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
W. R. Grace & Co.-Conn.
-
NDC:
22568-8865
-
Nonproprietary Name:
Amifostine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
AMIFOSTINE
-
Start Marketing Date:
2021-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Wacker Biotech GmbH
-
NDC:
72820-100
-
Nonproprietary Name:
RETEPLASE
-
Dosage Form:
SOLUTION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
RETEPLASE
-
Start Marketing Date:
2017-06-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Wanbury Limted
-
NDC:
62350-0079
-
Nonproprietary Name:
DOCUSATE SODIUM
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DOCUSATE SODIUM
-
Start Marketing Date:
2017-05-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
63155-1034
-
Nonproprietary Name:
METFORMIN HYDROCHLORIDE DC
-
Dosage Form:
GRANULE
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
METFORMIN HYDROCHLORIDE
-
Start Marketing Date:
2021-01-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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