National Drug Code (NDC) Database
-
NDC:
62068-380
-
Nonproprietary Name:
Abiraterone Acetate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1000 g/1000g
-
Substance:
ABIRATERONE ACETATE
-
Start Marketing Date:
2013-03-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Willow Birch Pharma, Inc
-
NDC:
10695-175
-
Nonproprietary Name:
TadalafilUSP
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TADALAFIL
-
Start Marketing Date:
2024-08-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Willow Birch Pharma, Inc.
-
NDC:
10695-311
-
Nonproprietary Name:
Topiramate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TOPIRAMATE
-
Start Marketing Date:
2025-08-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Willow Birch Pharma, Inc/
-
NDC:
10695-114
-
Nonproprietary Name:
Naltrexone HCL
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NALTREXONE HYDROCHLORIDE
-
Start Marketing Date:
2025-02-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Willow Birch Pharma, LLC
-
NDC:
10695-337
-
Nonproprietary Name:
Rosuvastatin Calcium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ROSUVASTATIN CALCIUM
-
Start Marketing Date:
2026-05-04
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Willow Birch Pharma, LLC.
-
NDC:
10695-340
-
Nonproprietary Name:
Cyclophosphamide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CYCLOPHOSPHAMIDE
-
Start Marketing Date:
2026-06-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
13612-0013
-
Nonproprietary Name:
Tulathromycin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TULATHROMYCIN
-
Start Marketing Date:
2015-12-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Wisdom Pharmaceutical Co.,Ltd
-
NDC:
13612-0032
-
Nonproprietary Name:
Baricitinib
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BARICITINIB
-
Start Marketing Date:
2025-05-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Wisdom Pharmaceutical Co.,Ltd.
-
NDC:
13612-0024
-
Nonproprietary Name:
Aprepitant
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
APREPITANT
-
Start Marketing Date:
2021-10-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Wugan Pharmaceutical (Suzhou) Co., Ltd.
-
NDC:
86129-0002
-
Nonproprietary Name:
Sulfadiazine Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SULFADIAZINE SODIUM
-
Start Marketing Date:
2020-08-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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