National Drug Code (NDC) Database
Dongguan Shenglian Tins Products Co., Ltd.
-
NDC:
84956-015
-
Nonproprietary Name:
HYDROCORTISONE
-
Dosage Form:
KIT
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
-
Substance:
-
Start Marketing Date:
2025-04-01
-
End Marketing Date:
2026-12-31
-
DEA Schedule:
-
Certified Through:
0000-00-00
Dow Benelux B.V.
-
NDC:
87289-4003
-
Nonproprietary Name:
Polyethylene Glycol 4000
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
POLYETHYLENE GLYCOL 4000
-
Start Marketing Date:
2026-04-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Dr Reddy's Laboratories Inc.
-
NDC:
75907-099
-
Nonproprietary Name:
brimonidine tartrate
-
Dosage Form:
SOLUTION/ DROPS
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.25 mg/mL
-
Substance:
BRIMONIDINE TARTRATE
-
Start Marketing Date:
2024-02-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Dr Reddy's Laboratories Limited
-
NDC:
55111-044
-
Nonproprietary Name:
Lansoprazole
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LANSOPRAZOLE
-
Start Marketing Date:
2008-03-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
DR REDDY¿S LABORATORIES (EU) LTD
-
NDC:
55359-540
-
Nonproprietary Name:
Travoprost
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TRAVOPROST
-
Start Marketing Date:
2013-09-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Dr Reddy’s Laboratories Limited
-
NDC:
71796-059
-
Nonproprietary Name:
Cabozantinib Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CABOZANTINIB
-
Start Marketing Date:
2023-03-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Dr. Reddy's Laboratories Inc.
-
NDC:
75907-374
-
Nonproprietary Name:
Zoliflodacin
-
Dosage Form:
GRANULE
-
Product Type:
BULK INGREDIENT
-
Strength:
3 g/3g
-
Substance:
ZOLIFLODACIN
-
Start Marketing Date:
2026-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Dr. Reddy's Laboratories Limited
-
NDC:
71796-068
-
Nonproprietary Name:
Nicotinamide Riboside
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 kg/1
-
Substance:
NICOTINAMIDE RIBOSIDE CHLORIDE
-
Start Marketing Date:
2024-03-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
54864-874
-
Nonproprietary Name:
Selumetinib Hyd Sulfate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SELUMETINIB SULFATE
-
Start Marketing Date:
2020-04-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
58243-477
-
Nonproprietary Name:
Norethindrone Acetate And Ethinyl Estradiol Capsules And Ferrous Fumarate Capsules, 1 MG/20 MCG
-
Dosage Form:
CAPSULE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
.02; 1 mg/1; mg/1
-
Substance:
ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
-
Start Marketing Date:
2021-05-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Create a New Buying Request
Fields marked with * are mandatory.