National Drug Code (NDC) Database
ROVI Pharma Industrial Services S.A.
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NDC:
68263-012
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Nonproprietary Name:
Moderna COVID-19 Vaccine
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Dosage Form:
INJECTION, SUSPENSION
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Product Type:
VACCINE
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Strength:
25 ug/.25mL
-
Substance:
CX-046684
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Start Marketing Date:
2024-08-20
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
RUBAMIN PRIVATE LIMITED
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NDC:
87620-001
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Nonproprietary Name:
Zinc Oxide 25
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Dosage Form:
BEAD
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Product Type:
BULK INGREDIENT
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Strength:
10 kg/10kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2026-04-17
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Rui Laboratories private limited
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NDC:
81414-001
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Nonproprietary Name:
Levetiracetam
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LEVETIRACETAM
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Start Marketing Date:
2021-02-02
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Ruyuan HEC Pharm Co., Ltd.
-
NDC:
70232-0012
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Nonproprietary Name:
Fingolimod Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
FINGOLIMOD HYDROCHLORIDE
-
Start Marketing Date:
2021-11-26
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
S&B Pharma LLC dba Norac Pharma
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NDC:
53834-701
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Nonproprietary Name:
Tapentadol Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TAPENTADOL HYDROCHLORIDE
-
Start Marketing Date:
2025-11-04
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CII
-
Certified Through:
2027-12-31
S.A.L.A.R.S. SOCIETà AZIONARIA LABORATORI ALCALOIDI RIFORNIMENTI SANITARI S.P.A.
-
NDC:
69641-0002
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Nonproprietary Name:
Naltrexone
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NALTREXONE
-
Start Marketing Date:
2015-02-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
SAB HERBALS AND NUTRACEUTICALS
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NDC:
81795-001
-
Nonproprietary Name:
Senna Dry Extract
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
20 kg/20kg
-
Substance:
SENNOSIDES
-
Start Marketing Date:
2021-04-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
SAFIR TUZ GIDA MADEN PAZARLAMA NAKLIYAT INSAAT ITHALAT IHRACAT SANAYI VE TICARET ANONIM SIRKETI CERIKLI RAFINE TUZ TESISI SUBESI
-
NDC:
87020-002
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Nonproprietary Name:
SODIUM CHLORIDE
-
Dosage Form:
GRANULE
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SODIUM CHLORIDE
-
Start Marketing Date:
2025-07-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
68263-674
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Nonproprietary Name:
alendronate sodium and cholecalciferol
-
Dosage Form:
TABLET
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
70; 5600 mg/30kg; [iU]/30kg
-
Substance:
ALENDRONATE SODIUM; CHOLECALCIFEROL
-
Start Marketing Date:
2021-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
70312-0891
-
Nonproprietary Name:
Nalbuphine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
NALBUPHINE HYDROCHLORIDE
-
Start Marketing Date:
2026-04-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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