NDC codes

FDA NDC Directory
Product NDC (as listed)23155-971Labeler and product segments. Claims need a package NDC.
Product NDC at billing width23155-0971Add 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 NDC11-digit (billing)PackageCopy
23155-971-0123155097101100 TABLET in 1 BOTTLE (23155-971-01)Marketed from Mar 25, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076725
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)
Identifiers
Product ID 23155-971_4d5e3859-0e0a-810d-e063-6294a90af18cSPL ID 4d5e3859-0e0a-810d-e063-6294a90af18cSPL set ID 4d5e42be-3476-85d4-e063-6294a90a0865RxCUI 993462, 993466, 993470UNII 59JV96YTXVUPC 0323155969016, 0323155970012, 0323155971019
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

N423155097101 followed by a unit qualifier and the quantity

Package 23155-0971-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 076725

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

FDA NDC Directory listings under ANDA 076725
ProductStrengthForm · routeLabelerProduct NDC
Midodrine HydrochlorideMidodrine hydrochloride 2.5 mg/1TabletOralAvet Pharmaceuticals Inc.23155-969
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralAvet Pharmaceuticals Inc.23155-970
Midodrine HydrochlorideMidodrine hydrochloride 2.5 mg/1TabletOralUpsher-Smith laboratories, LLC0245-0211
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralUpsher-Smith laboratories, LLC0245-0212
Midodrine HydrochlorideMidodrine hydrochloride 10 mg/1TabletOralUpsher-Smith laboratories, LLC0245-0213
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralCardinal Health 107, LLC55154-5623

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