What is NDC 55154-4174?

55154-4174 is the product NDC for Midodrine Hydrochloride, Midodrine hydrochloride 10 mg/1 tablet, listed with the FDA by Cardinal Health 107, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Cardinal Health 107, LLC, NDC labeler code 55154. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Midodrine Hydrochloride?

108 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Midodrine Hydrochloride NDC 55154-4174

NDC codes

FDA NDC Directory

Product NDC (as listed)55154-4174Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55154-4174Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
55154-4174-6	5515441740655154417406	6 BLISTER PACK in 1 BAG (55154-4174-6) / 1 TABLET in 1 BLISTER PACKMarketed from Sep 12, 2006

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Midodrine Hydrochloride
Generic name (nonproprietary): midodrine hydrochloride
Active ingredients: Midodrine hydrochloride — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Cardinal Health 107, LLCNDC labeler code 55154
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077746
Marketing start: Sep 12, 2006
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)
Identifiers: Product ID 55154-4174_56df3d55-68c0-44ef-ae77-26b7abfa7811SPL ID 56df3d55-68c0-44ef-ae77-26b7abfa7811SPL set ID 5e2443c2-f714-4b1d-bf2d-22742f411961RxCUI 993462, 993470UNII 59JV96YTXVUPC 0055154417464
Pharmacologic class: alpha-Adrenergic Agonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N455154417406 followed by a unit qualifier and the quantity

Package 55154-4174-06. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Nov 3, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Midodrine hydrochloride is indicated for the treatment of symptomatic orthostatic hypotension (OH). Because midodrine hydrochloride can cause marked elevation of supine blood pressure (BP>200 mmHg systolic), it should be used in patients whose lives are considerably impaired despite standard clinical care, including non-pharmacologic treatment (such as support stockings), fluid expansion, and lifestyle alterations. The indication is based on midodrine hydrochloride's effect on increases in 1-minute standing systolic blood pressure, a surrogate marker considered likely to correspond to a clinical benefit. At present, however, clinical benefits of midodrine hydrochloride,…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55154-4174

What is NDC 55154-4174?: 55154-4174 is the product NDC for Midodrine Hydrochloride, Midodrine hydrochloride 10 mg/1 tablet, listed with the FDA by Cardinal Health 107, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Midodrine Hydrochloride.
What is the active ingredient?: Midodrine hydrochloride.
Who is the labeler?: Cardinal Health 107, LLC, NDC labeler code 55154. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Midodrine Hydrochloride?: 108 other product NDCs are listed under this name. See all Midodrine Hydrochloride NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Midodrine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	Major Pharmaceuticals	0904-7640	00904-7640-0600904-7640-61
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	Major Pharmaceuticals	0904-7641	00904-7641-0600904-7641-61
Midodrine Hydrochloride	Midodrine hydrochloride 10 mg/1	TabletOral	Major Pharmaceuticals	0904-7642	00904-7642-07
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	NorthStar RxLLC	72603-906	72603-0906-0572603-0906-10
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	NorthStar RxLLC	72603-907	72603-0907-0572603-0907-10
Midodrine Hydrochloride	Midodrine hydrochloride 10 mg/1	TabletOral	NorthStar RxLLC	72603-908	72603-0908-0372603-0908-05
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	Avet Pharmaceuticals Inc.	23155-969	23155-0969-01
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	Avet Pharmaceuticals Inc.	23155-970	23155-0970-01
Midodrine Hydrochloride	Midodrine hydrochloride 10 mg/1	TabletOral	Avet Pharmaceuticals Inc.	23155-971	23155-0971-01
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	Safecor Health LLC	48433-075	48433-0075-20

All 109 Midodrine Hydrochloride NDCs

Other NDCs under ANDA 077746

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 077746
Product	Strength	Form · route	Labeler	Product NDC
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	Major Pharmaceuticals	0904-6817
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	Major Pharmaceuticals	0904-6818
Midodrine Hydrochloride	Midodrine hydrochloride 10 mg/1	TabletOral	Major Pharmaceuticals	0904-6819
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	AvKARE	42291-560
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	AvKARE	42291-561
Midodrine Hydrochloride	Midodrine hydrochloride 10 mg/1	TabletOral	AvKARE	42291-562
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	AvPAK	50268-561
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	AvPAK	50268-562
Midodrine Hydrochloride	Midodrine hydrochloride 10 mg/1	TabletOral	AvPAK	50268-563
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	Cardinal Health 107, LLC	55154-8086
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	Apotex Corp	60505-1320
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	Apotex Corp	60505-1321
Midodrine Hydrochloride	Midodrine hydrochloride 10 mg/1	TabletOral	Apotex Corp	60505-1325
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	American Health Packaging	60687-387
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	American Health Packaging	60687-398
Midodrine Hydrochloride	Midodrine hydrochloride 10 mg/1	TabletOral	American Health Packaging	60687-409
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	Bryant Ranch Prepack	71335-1433