National Drug Code (NDC) Database
Amneal Pharmaceuticals Co. (I) Pvt. Ltd.
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NDC:
52493-903
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Nonproprietary Name:
TELMISARTAN
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Dosage Form:
GRANULE
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Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TELMISARTAN
-
Start Marketing Date:
2024-07-20
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
AMOL PHARMACEUTICALS PRIVATE LIMITED
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NDC:
63189-025
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Nonproprietary Name:
Sennosides
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Dosage Form:
TABLET
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
17.2 mg/1
-
Substance:
SENNOSIDES
-
Start Marketing Date:
2026-01-01
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Amoli Organics (A Division of Umedica Laboratories Private Limited)
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NDC:
62512-0056
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Nonproprietary Name:
Tadalafil
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TADALAFIL
-
Start Marketing Date:
2017-11-29
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Amoli Organics (A Division of Umedica Laboratories Pvt.Ltd)
-
NDC:
62512-0083
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Nonproprietary Name:
SITAGLIPTIN ANHYDR0US
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
SITAGLIPTIN PHOSPHATE ANHYDROUS
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Start Marketing Date:
2024-01-07
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Amoli Organics (A Division of Umedica Laboratories Pvt.Ltd.)
-
NDC:
62512-0081
-
Nonproprietary Name:
Mirabegron
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MIRABEGRON
-
Start Marketing Date:
2024-03-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Amphastar France Pharmaceuticals
-
NDC:
69098-101
-
Nonproprietary Name:
Recombinant Human Insulin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
INSULIN HUMAN
-
Start Marketing Date:
2014-07-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Amphastar France Pharmaceuticals, Inc.
-
NDC:
69098-101
-
Nonproprietary Name:
Recombinant Human Insulin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
INSULIN HUMAN
-
Start Marketing Date:
2014-07-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Amphastar Nanjing Pharmaceuticals
-
NDC:
52221-109
-
Nonproprietary Name:
Salmeterol Xinafoate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
0.4 kg/.4kg
-
Substance:
SALMETEROL XINAFOATE
-
Start Marketing Date:
2014-09-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Amphastar Nanjing Pharmaceuticals, Inc.
-
NDC:
52221-201
-
Nonproprietary Name:
Hyaluronidase
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
HYALURONIDASE
-
Start Marketing Date:
2015-06-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
62512-0085
-
Nonproprietary Name:
Sacubitril/Valsartan
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SACUBITRIL VALSARTAN
-
Start Marketing Date:
2025-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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