National Drug Code (NDC) Database
Symrise Inc.
-
NDC:
50765-7643
-
Nonproprietary Name:
Menthol Racemic
-
Dosage Form:
CONCENTRATE
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
RACEMENTHOL
-
Start Marketing Date:
2025-04-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Symrise, Inc.
-
NDC:
50765-6125
-
Nonproprietary Name:
Levomenthol
-
Dosage Form:
CONCENTRATE
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LEVOMENTHOL
-
Start Marketing Date:
2023-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Symrise, S. DE R.L.DE C.V.
-
NDC:
67270-101
-
Nonproprietary Name:
OCTISALATE
-
Dosage Form:
CONCENTRATE
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
OCTISALATE
-
Start Marketing Date:
2002-07-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Syn-Tech Chem. & Pharm. Co. LTD.
-
NDC:
54871-1097
-
Nonproprietary Name:
Epinephrine Bitartrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
EPINEPHRINE BITARTRATE
-
Start Marketing Date:
2016-06-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Syn-Tech Chem. & Pharm. Co., Ltd.
-
NDC:
54871-1099
-
Nonproprietary Name:
Xylazine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
XYLAZINE HYDROCHLORIDE
-
Start Marketing Date:
2025-01-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Synergene Active Ingredients Private Limited
-
NDC:
60695-006
-
Nonproprietary Name:
Tadalafil
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TADALAFIL
-
Start Marketing Date:
2024-08-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Synergy Health
-
NDC:
71161-152
-
Nonproprietary Name:
birch triterpenes
-
Dosage Form:
GEL
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100 mg/g
-
Substance:
BIRCH TRITERPENES
-
Start Marketing Date:
2024-02-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Synergy Health AST
-
NDC:
71161-157
-
Nonproprietary Name:
Leuprolide Acetate
-
Dosage Form:
INJECTION, SUSPENSION, EXTENDED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
45 mg/.375mL
-
Substance:
LEUPROLIDE ACETATE
-
Start Marketing Date:
2026-03-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Synergy Health AST, Inc
-
NDC:
71161-106
-
Nonproprietary Name:
triptorelin
-
Dosage Form:
INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
22.5 mg/2mL
-
Substance:
TRIPTORELIN
-
Start Marketing Date:
2017-09-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
63622-0125
-
Nonproprietary Name:
Amphotericin B
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
5 kg/5kg
-
Substance:
AMPHOTERICIN B
-
Start Marketing Date:
2019-08-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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