National Drug Code (NDC) Database
Norbitec GmbH
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NDC:
83063-015
-
Nonproprietary Name:
Epoetin
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
2.8 g/2.8g
-
Substance:
EPOETIN
-
Start Marketing Date:
2023-03-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Nordmark Pharma GmbH
-
NDC:
81618-0004
-
Nonproprietary Name:
Thyroid, Porcine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
THYROID
-
Start Marketing Date:
2019-08-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Nortec Quimica S.A.
-
NDC:
59014-0052
-
Nonproprietary Name:
Prilocaine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
10 kg/10kg
-
Substance:
PRILOCAINE
-
Start Marketing Date:
2017-09-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
North China Pharmaceutical Co., Ltd. Beta Branch Factory
-
NDC:
87488-101
-
Nonproprietary Name:
Penicillin G Potassium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PENICILLIN G POTASSIUM
-
Start Marketing Date:
2026-03-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
North China Pharmaceutical Huasheng Co. Ltd.
-
NDC:
55500-0011
-
Nonproprietary Name:
Sirolimus
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SIROLIMUS
-
Start Marketing Date:
2019-07-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
NORTHERN LABS, INC.
-
NDC:
83477-516
-
Nonproprietary Name:
Benzalkonium Chloride
-
Dosage Form:
SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1.45 g/L
-
Substance:
BENZALKONIUM CHLORIDE
-
Start Marketing Date:
2026-03-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Nouryon Chemicals, S.A. de C.V.
-
NDC:
67645-347
-
Nonproprietary Name:
BENZOYL PEROXIDE
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
35 kg/100kg
-
Substance:
BENZOYL PEROXIDE
-
Start Marketing Date:
2009-04-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
59014-0053
-
Nonproprietary Name:
Bupivacaine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
BUPIVACAINE
-
Start Marketing Date:
2018-04-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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