National Drug Code (NDC) Database
Hangzhou Jodomi Biotech Co.,Ltd
-
NDC:
87173-765
-
Nonproprietary Name:
semaglutide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
SEMAGLUTIDE
-
Start Marketing Date:
2025-10-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
60723-207
-
Nonproprietary Name:
ALENDRONATE SODIUM
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
35 mg/1
-
Substance:
ALENDRONATE SODIUM
-
Start Marketing Date:
2018-01-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Hangzhou XinHan Biopharma Co., Ltd.
-
NDC:
84789-117
-
Nonproprietary Name:
Thymalfasin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
THYMALFASIN
-
Start Marketing Date:
2025-12-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hangzhou Yiqi Biotechnology Co., Ltd
-
NDC:
85139-021
-
Nonproprietary Name:
KPV acetate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
100 g/100g
-
Substance:
PEPTIDE B27PD
-
Start Marketing Date:
2025-07-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hangzhou Younger International Co.,ltd
-
NDC:
85093-001
-
Nonproprietary Name:
tirzepatide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
100 g/100g
-
Substance:
TIRZEPATIDE
-
Start Marketing Date:
2025-01-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd
-
NDC:
65897-3010
-
Nonproprietary Name:
Tacrolimus
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TACROLIMUS
-
Start Marketing Date:
2022-01-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.
-
NDC:
65897-4005
-
Nonproprietary Name:
Acarbose
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ACARBOSE
-
Start Marketing Date:
2022-12-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hanil Chemical Ind. Co., Ltd.
-
NDC:
73174-050
-
Nonproprietary Name:
Zinc Oxide
-
Dosage Form:
POWDER
-
Product Type:
HUMAN OTC DRUG
-
Strength:
0.995 kg/kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2020-11-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hanmi Pharm. Co., Ltd.
-
NDC:
83089-101
-
Nonproprietary Name:
EFLAPEGRASTIM
-
Dosage Form:
SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
33.4 g/L
-
Substance:
EFLAPEGRASTIM
-
Start Marketing Date:
2022-09-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Hanseler AG
-
NDC:
69955-5005
-
Nonproprietary Name:
Olbas Analgesic Salve
-
Dosage Form:
SALVE
-
Product Type:
BULK INGREDIENT
-
Strength:
6.525 kg/6.525kg
-
Substance:
PEPPERMINT OIL
-
Start Marketing Date:
1970-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Create a New Buying Request
Fields marked with * are mandatory.