National Drug Code (NDC) Database
Chongqing Kangle Pharmaceutical Co., Ltd.
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NDC:
67680-003
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Nonproprietary Name:
Hydroxychloroquine Sulfate
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
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Substance:
HYDROXYCHLOROQUINE SULFATE
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Start Marketing Date:
2017-11-21
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Chongqing Kangle Pharmaceutical Co.,Ltd.
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NDC:
67680-002
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Nonproprietary Name:
TIGECYCLINE
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
TIGECYCLINE
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Start Marketing Date:
2014-01-10
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Chongqing Qiancan Technology Co., LTD
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NDC:
87095-001
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Nonproprietary Name:
Enclomiphene Citrate
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
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Strength:
1 g/g
-
Substance:
ENCLOMIPHENE
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Start Marketing Date:
2025-09-09
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Chongqing Sintaho Pharmaceutical Co., Ltd.
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NDC:
84172-901
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Nonproprietary Name:
Eribulin Mesylate
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Dosage Form:
INJECTION, SOLUTION
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Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
ERIBULIN MESYLATE
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Start Marketing Date:
2024-07-01
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Chongqing Southwest No.2 Pharmaceutical Factory Co., Ltd.
-
NDC:
20362-0585
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Nonproprietary Name:
Procaine Hydrochloride
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
PROCAINE HYDROCHLORIDE
-
Start Marketing Date:
2011-11-21
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2027-12-31
Chongqing Dijiasuo Pharmaceutical Technology Co., Ltd.
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NDC:
85389-002
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Nonproprietary Name:
Nitazoxanide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
NITAZOXANIDE
-
Start Marketing Date:
2025-06-17
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Chonqing Sintaho Pharmaceutical Co., Ltd.
-
NDC:
84172-123
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Nonproprietary Name:
Orforglipron Calcium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ORFORGLIPRON CALCIUM
-
Start Marketing Date:
2026-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Chr. Olesen Synthesis A/S
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NDC:
82274-001
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Nonproprietary Name:
Buprenorphine Hydrochloride
-
Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BUPRENORPHINE HYDROCHLORIDE
-
Start Marketing Date:
2024-12-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CIII
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Certified Through:
2027-12-31
Chromo Laboratories India Private Limited
-
NDC:
52562-801
-
Nonproprietary Name:
ZAFIRLUKAST
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ZAFIRLUKAST
-
Start Marketing Date:
2013-11-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Chugai Pharmaceutical Co., Ltd.
-
NDC:
60422-402
-
Nonproprietary Name:
Nemolizumab
-
Dosage Form:
LIQUID
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
100 mg/.001L
-
Substance:
NEMOLIZUMAB
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Start Marketing Date:
2024-08-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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