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Emicizumab NDCs, Package Codes, Strengths & Labelers

This page lists NDC package records for Emicizumab products — strengths, dosage forms, package sizes, labelers, 11-digit billing NDCs, pricing data when available, and links to each individual NDC page. It’s an NDC/package & billing directory, not a clinical drug page.

Looking for uses, warnings & side effects? Read our Emicizumab drug information page →

Key stats

18
Package NDCs
17
Products
17
Active listings
0
Discontinued
4
Labelers
13
Strengths
3
Dosage forms
0
With NADAC pricing

By strength, form & labeler

NDC products by strength
EMICIZUMAB 150 mg/mL 2
EMICIZUMAB 30 mg/mL 2
EMICIZUMAB 105 mg/.7mL 2
EMICIZUMAB 60 mg/.4mL 2
EMICIZUMAB 150 mg/1 1
EMICIZUMAB 150 mg/.001L 1
EMICIZUMAB 60 mg/1 1
EMICIZUMAB 105 mg/1 1
EMICIZUMAB 300 mg/2mL 1
EMICIZUMAB-KXWH 300 mg/2mL 1
By dosage form
INJECTION, SOLUTION 12
SOLUTION 4
LIQUID 1
Top labelers
Genentech, Inc. 6
Chugai Pharmaceutical Co., Ltd. 5
SAMSUNG BIOLOGICS Co., Ltd. 4
Samsung BioLogics Co. LTD 2

Browse records — 17 products

Drug / product Billing NDC NADAC / unit Status
Emicizumab 150 mg/1 SOLUTION SAMSUNG · NDC 71124-0012-00 · 1 SOLUTION in 1 VIAL, SINGLE-USE (71124-0012-0) 71124-0012-00 On market View →
Emicizumab 30 mg/mL INJECTION, SOLUTION Chugai · NDC 60422-0260-01 · 1 VIAL, SINGLE-USE in 1 CARTON (60422-260-01) / 1 mL in 1 VIAL, SINGLE-USE 60422-0260-01 On market View →
Emicizumab 150 mg/.001L LIQUID Chugai · NDC 60422-0302-01 · 2 L in 1 BAG (60422-302-01) 60422-0302-01 On market View →
Emicizumab 60 mg/1 SOLUTION SAMSUNG · NDC 71124-0010-00 · 1 SOLUTION in 1 VIAL, SINGLE-USE (71124-0010-0) 71124-0010-00 On market View →
Emicizumab 105 mg/1 SOLUTION SAMSUNG · NDC 71124-0011-00 · 1 SOLUTION in 1 VIAL, SINGLE-USE (71124-0011-0) 71124-0011-00 On market View →
emicizumab 300 mg/2mL INJECTION, SOLUTION Samsung · NDC 71124-0054-00 · 2 mL in 1 VIAL, GLASS (71124-0054-0) 71124-0054-00 On market View →
Emicizumab 30 mg/1 SOLUTION SAMSUNG · NDC 71124-0009-00 · 1 SOLUTION in 1 VIAL, SINGLE-USE (71124-0009-0) 71124-0009-00 On market View →
Emicizumab 105 mg/.7mL INJECTION, SOLUTION Chugai · NDC 60422-0280-01 · 1 VIAL, SINGLE-USE in 1 CARTON (60422-280-01) / .7 mL in 1 VIAL, SINGLE-USE 60422-0280-01 On market View →
Emicizumab 60 mg/.4mL INJECTION, SOLUTION Chugai · NDC 60422-0270-01 · 1 VIAL, SINGLE-USE in 1 CARTON (60422-270-01) / .4 mL in 1 VIAL, SINGLE-USE 60422-0270-01 On market View →
Emicizumab 150 mg/mL INJECTION, SOLUTION Chugai · NDC 60422-0290-01 · 1 VIAL, SINGLE-USE in 1 CARTON (60422-290-01) / 1 mL in 1 VIAL, SINGLE-USE 60422-0290-01 On market View →
emicizumab 12 mg/.4mL INJECTION, SOLUTION Samsung · NDC 71124-0057-00 · .4 mL in 1 VIAL, GLASS (71124-0057-0) 71124-0057-00 On market View →
Hemlibra emicizumab 150 mg/mL INJECTION, SOLUTION Genentech, · NDC 50242-0923-01 · J7170 · 1 VIAL, SINGLE-USE in 1 CARTON (50242-923-01) / 1 mL in 1 VIAL, SINGLE-USE 50242-0923-01 On market View →
Hemlibra emicizumab 105 mg/.7mL INJECTION, SOLUTION Genentech, · NDC 50242-0922-01 · J7170 · 1 VIAL, SINGLE-USE in 1 CARTON (50242-922-01) / .7 mL in 1 VIAL, SINGLE-USE 50242-0922-01 On market View →
Hemlibra emicizumab 300 mg/2mL INJECTION, SOLUTION Genentech, · NDC 50242-0930-01 · J7170 · 1 VIAL, SINGLE-USE in 1 CARTON (50242-930-01) / 2 mL in 1 VIAL, SINGLE-USE 50242-0930-01 On market View →
Hemlibra emicizumab 60 mg/.4mL INJECTION, SOLUTION Genentech, · NDC 50242-0921-01 · J7170 · 1 VIAL, SINGLE-USE in 1 CARTON (50242-921-01) / .4 mL in 1 VIAL, SINGLE-USE 50242-0921-01 On market View →
Hemlibra emicizumab 12 mg/.4mL INJECTION, SOLUTION Genentech, · NDC 50242-0927-01 · J7170 · 1 VIAL, SINGLE-USE in 1 CARTON (50242-927-01) / .4 mL in 1 VIAL, SINGLE-USE 50242-0927-01 On market View →
Hemlibra emicizumab 30 mg/mL INJECTION, SOLUTION Genentech, · NDC 50242-0920-01 · J7170 · 1 VIAL, SINGLE-USE in 1 CARTON (50242-920-01) / 1 mL in 1 VIAL, SINGLE-USE 50242-0920-01 On market View →
Where does this data come from?
NDC package records, strengths, forms and labelers come from the openFDA NDC Directory; pricing is CMS NADAC. Grouped by active-ingredient name. This is package/billing reference data, not clinical drug information.