National Drug Code (NDC) Database
Xenex Laboratories Inc
-
NDC:
68981-046
-
Nonproprietary Name:
PHENAZOPYRIDINE HCL
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
PHENAZOPYRIDINE HYDROCHLORIDE
-
Start Marketing Date:
2021-04-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Xenova Sciences, LLC
-
NDC:
83162-001
-
Nonproprietary Name:
Thyroid Powder
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
THYROID, UNSPECIFIED
-
Start Marketing Date:
2023-10-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Xiamen Tiger Medical Company, Ltd
-
NDC:
51080-215
-
Nonproprietary Name:
Camphor (Synthetic) and MENTHOL, UNSPECIFIED FORM
-
Dosage Form:
OINTMENT
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
110; 110 g/kg; g/kg
-
Substance:
CAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM
-
Start Marketing Date:
2024-02-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
70203-101
-
Nonproprietary Name:
CONJUGATED ESTROGENS
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
80 mg/80mg
-
Substance:
ESTROGENS, CONJUGATED
-
Start Marketing Date:
2015-12-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Xinyu Pharmaceutical Co.,Ltd
-
NDC:
42881-0001
-
Nonproprietary Name:
lincomycin hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LINCOMYCIN HYDROCHLORIDE
-
Start Marketing Date:
2017-12-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
0116-0100
-
Nonproprietary Name:
Chlorhexidine Gluconate 20% Solution
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
20 g/20g
-
Substance:
CHLORHEXIDINE
-
Start Marketing Date:
1985-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Yabao Pharmaceutical Group Co., Ltd.
-
NDC:
69262-0002
-
Nonproprietary Name:
Sorafenib Tosylate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SORAFENIB TOSYLATE
-
Start Marketing Date:
2022-11-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Yancheng Suhai Pharmaceutical Co., Ltd.
-
NDC:
67698-101
-
Nonproprietary Name:
DOXYCYCLINE HYCLATE
-
Dosage Form:
POWDER, FOR SUSPENSION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DOXYCYCLINE HYCLATE
-
Start Marketing Date:
2015-09-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
YANGZHOU LIBERTY PHARMACEUTICAL CO. LTD
-
NDC:
71057-3440
-
Nonproprietary Name:
DOXYCYCLINE HYCLATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DOXYCYCLINE ANHYDROUS
-
Start Marketing Date:
2016-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
61046-0003
-
Nonproprietary Name:
Gramicidin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
GRAMICIDIN
-
Start Marketing Date:
2004-07-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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