National Drug Code (NDC) Database
Dr. Reddy's Laboratories Ltd.
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NDC:
71796-002
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Nonproprietary Name:
Empagliflozin Amorphous
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
EMPAGLIFLOZIN
-
Start Marketing Date:
2018-03-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Dr. Reddys Laboratories Inc
-
NDC:
75907-119
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Nonproprietary Name:
Esomeprazole Magnesium
-
Dosage Form:
TABLET, DELAYED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
20 mg/1
-
Substance:
ESOMEPRAZOLE MAGNESIUM
-
Start Marketing Date:
2023-11-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Dr. Reddys laboratories Limited
-
NDC:
71796-006
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Nonproprietary Name:
Dapagliflozin Propanediol
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DAPAGLIFLOZIN PROPANEDIOL
-
Start Marketing Date:
2018-08-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Dr. Reddy¿s Laboratories Inc.
-
NDC:
43598-407
-
Nonproprietary Name:
Esomeprazole Magnesium
-
Dosage Form:
CAPSULE, DELAYED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
20 mg/1
-
Substance:
ESOMEPRAZOLE MAGNESIUM
-
Start Marketing Date:
2025-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Dr. Reddy¿s Laboratories Limited
-
NDC:
71796-031
-
Nonproprietary Name:
Hydroxychloroquine Sulfate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
HYDROXYCHLOROQUINE SULFATE
-
Start Marketing Date:
2021-02-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Dr. Reddy¿s Laboratories Ltd.
-
NDC:
55111-060
-
Nonproprietary Name:
Sumatriptan Succinate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SUMATRIPTAN SUCCINATE
-
Start Marketing Date:
2003-03-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Dr. Reddy’s Laboratories Limited
-
NDC:
71796-049
-
Nonproprietary Name:
Bempedoic Acid
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BEMPEDOIC ACID
-
Start Marketing Date:
2022-03-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Dr.Reddy's Laboratoriees Limited
-
NDC:
55111-057
-
Nonproprietary Name:
Ramipril
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
RAMIPRIL
-
Start Marketing Date:
2002-10-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Dr.Reddy's Laboratories Inc
-
NDC:
43598-892
-
Nonproprietary Name:
Fexofenadine HCl and Pseudoephedrine HCl
-
Dosage Form:
TABLET, EXTENDED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
180; 240 mg/1; mg/1
-
Substance:
FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
-
Start Marketing Date:
2022-05-17
-
End Marketing Date:
2026-08-31
-
DEA Schedule:
-
Certified Through:
0000-00-00
Dr.Reddy's Laboratories Limited
-
NDC:
71796-066
-
Nonproprietary Name:
BELUMOSUDIL
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 kg/1
-
Substance:
BELUMOSUDIL
-
Start Marketing Date:
2021-07-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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