National Drug Code (NDC) Database
Synergy Health AST, LLC
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NDC:
71161-154
-
Nonproprietary Name:
cabotegravir and rilpivirine
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Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
300 mg/300mg
-
Substance:
RILPIVIRINE
-
Start Marketing Date:
2025-03-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Synergy Health, LLC
-
NDC:
71161-135
-
Nonproprietary Name:
triamcinolone acetonide
-
Dosage Form:
INJECTION, POWDER, FOR SUSPENSION, EXTENDED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
32 mg/1
-
Substance:
TRIAMCINOLONE ACETONIDE
-
Start Marketing Date:
2017-10-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Synfine Drugs Private Limited
-
NDC:
83875-005
-
Nonproprietary Name:
METRONIDAZOLE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
METRONIDAZOLE
-
Start Marketing Date:
2026-05-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Syntese A/S
-
NDC:
24528-0003
-
Nonproprietary Name:
Mesalamine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MESALAMINE
-
Start Marketing Date:
2006-07-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
51364-0007
-
Nonproprietary Name:
Ergocalciferol
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
ERGOCALCIFEROL
-
Start Marketing Date:
1994-10-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Synthimed Labs Private Limited
-
NDC:
65096-0117
-
Nonproprietary Name:
Anastrozole
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ANASTROZOLE
-
Start Marketing Date:
2010-12-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Synthokem Labs Private Limited
-
NDC:
58343-0140
-
Nonproprietary Name:
Prazosin Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PRAZOSIN HYDROCHLORIDE
-
Start Marketing Date:
2022-10-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Synthokem Labs Private Linited
-
NDC:
58343-0134
-
Nonproprietary Name:
Guaifenesin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GUAIFENESIN
-
Start Marketing Date:
2026-02-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
84101-004
-
Nonproprietary Name:
Belinostat
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BELINOSTAT
-
Start Marketing Date:
2024-03-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
43579-011
-
Nonproprietary Name:
Tamsulosin Hydrochloride
-
Dosage Form:
CAPSULE, GELATIN COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.4 mg/1
-
Substance:
TAMSULOSIN HYDROCHLORIDE
-
Start Marketing Date:
2010-04-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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