National Drug Code (NDC) Database
BDR Lifesciences Private Limited
-
NDC:
76361-0004
-
Nonproprietary Name:
Relugolix
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
RELUGOLIX
-
Start Marketing Date:
2024-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
BEC CHEMICALS PRIVATE LIMITED
-
NDC:
76465-0001
-
Nonproprietary Name:
KETOPROFEN
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
KETOPROFEN
-
Start Marketing Date:
2025-05-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd.
-
NDC:
85270-001
-
Nonproprietary Name:
Cromolyn Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CROMOLYN SODIUM
-
Start Marketing Date:
2025-02-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Bell Pharmaceuticals, Inc.
-
NDC:
15579-840
-
Nonproprietary Name:
CARBAMIDE PEROXIDE
-
Dosage Form:
SOLUTION/ DROPS
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
65 mg/mL
-
Substance:
CARBAMIDE PEROXIDE
-
Start Marketing Date:
2023-03-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Belleview Bioscience LLC
-
NDC:
84447-010
-
Nonproprietary Name:
Magnesium Oxide
-
Dosage Form:
TABLET
-
Product Type:
BULK INGREDIENT
-
Strength:
400 mg/400mg
-
Substance:
MAGNESIUM OXIDE
-
Start Marketing Date:
2025-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Belleview Biosciences LLC
-
NDC:
84447-113
-
Nonproprietary Name:
Magnesium Hydroxide
-
Dosage Form:
SUSPENSION
-
Product Type:
BULK INGREDIENT
-
Strength:
16000000 mg/16000000mg
-
Substance:
MAGNESIUM HYDROXIDE
-
Start Marketing Date:
2025-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
bene pharmaChem GmbH & Co. KG
-
NDC:
42897-001
-
Nonproprietary Name:
Pentosan Polysulfte Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PENTOSAN POLYSULFATE SODIUM
-
Start Marketing Date:
1996-11-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
BeOne Medicines USA, Inc.
-
NDC:
72579-900
-
Nonproprietary Name:
zanubrutinib
-
Dosage Form:
CAPSULE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
80 mg/1
-
Substance:
ZANUBRUTINIB
-
Start Marketing Date:
2023-10-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
70829-000
-
Nonproprietary Name:
POTASSIUM NITRATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
POTASSIUM NITRATE
-
Start Marketing Date:
2020-01-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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