National Drug Code (NDC) Database
Granules Pharmaceuticals Inc.
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NDC:
70010-149
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Nonproprietary Name:
butalbital, acetaminophen and caffeine
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Dosage Form:
TABLET
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
325; 50; 40 mg/1; mg/1; mg/1
-
Substance:
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
-
Start Marketing Date:
2022-06-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CIII
-
Certified Through:
2026-12-31
GREEN WAVES PRIVATE LIMITED
-
NDC:
66620-600
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Nonproprietary Name:
Chlorpheniramine Maleate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CHLORPHENIRAMINE MALEATE
-
Start Marketing Date:
2025-11-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Grillo Zinc Powder GmbH
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NDC:
72955-320
-
Nonproprietary Name:
Zinc Oxide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
100 kg/100kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2026-04-23
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
GRINDEKS Joint Stock Company
-
NDC:
64189-1202
-
Nonproprietary Name:
oxytocin
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
400000 U/g
-
Substance:
OXYTOCIN
-
Start Marketing Date:
2008-06-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
GROUPEMENT INTERET PUBLIC ARRONAX
-
NDC:
72088-001
-
Nonproprietary Name:
Sr-82 strontium dichloride
-
Dosage Form:
SOLUTION
-
Product Type:
BULK INGREDIENT
-
Strength:
5 mg/5mg
-
Substance:
STRONTIUM CHLORIDE SR-82
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Start Marketing Date:
2018-02-21
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Guangdong Blue Treasure Pharmaceuticals Co. Ltd
-
NDC:
43384-001
-
Nonproprietary Name:
Pravastatin Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PRAVASTATIN SODIUM
-
Start Marketing Date:
2011-07-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Guangdong HEC Bio&Pharm Co., Ltd.
-
NDC:
84772-002
-
Nonproprietary Name:
Dulaglutide
-
Dosage Form:
SOLUTION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
DULAGLUTIDE
-
Start Marketing Date:
2025-03-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Guangdong Longfu Medicine Co., Ltd.
-
NDC:
85781-001
-
Nonproprietary Name:
TIRZEPATIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
10 g/10g
-
Substance:
TIRZEPATIDE
-
Start Marketing Date:
2025-06-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
GUANGDONG NEWDARIN BIOTECHNOLOGY CO., LTD.
-
NDC:
78772-002
-
Nonproprietary Name:
Staurosporine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
STAUROSPORINE
-
Start Marketing Date:
2024-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Guangdong ZetaPharmax Co., Ltd
-
NDC:
84795-006
-
Nonproprietary Name:
BPC-157
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
BPC-157
-
Start Marketing Date:
2025-11-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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