NDC codes

FDA NDC Directory
Product NDC (as listed)81469-141Labeler and product segments. Claims need a package NDC.
Product NDC at billing width81469-0141Add 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
81469-141-908146901419090 TABLET in 1 BOTTLE (81469-141-90)Marketed from Aug 13, 2025

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 217271
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)
Identifiers
Product ID 81469-141_6e30fa38-fd26-4d37-a5f4-9e044c383362SPL ID 6e30fa38-fd26-4d37-a5f4-9e044c383362SPL set ID 414cebaa-b87f-4d41-bc41-a77dcd3ea434RxCUI 993462, 993466, 993470UNII 59JV96YTXV
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

N481469014190 followed by a unit qualifier and the quantity

Package 81469-0141-90. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Midodrine hydrochloride tablets are indicated for the treatment of symptomatic orthostatic hypotension (OH). Because midodrine hydrochloride tablets 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 tablets'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…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 217271

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

FDA NDC Directory listings under ANDA 217271
ProductStrengthForm · routeLabelerProduct NDC
Midodrine HydrochlorideMidodrine hydrochloride 2.5 mg/1TabletOralFirst Nation Group, LLC81469-139
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralFirst Nation Group, LLC81469-140
Midodrine HydrochlorideMidodrine hydrochloride 2.5 mg/1TabletOralNorthStar RxLLC72603-906
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralNorthStar RxLLC72603-907
Midodrine HydrochlorideMidodrine hydrochloride 10 mg/1TabletOralNorthStar RxLLC72603-908
Midodrine HydrochlorideMidodrine hydrochloride 2.5 mg/1TabletOralLifestar Pharma LLC70756-010
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralCoupler LLC67046-1512
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralLifestar Pharma LLC70756-049
Midodrine HydrochlorideMidodrine hydrochloride 10 mg/1TabletOralLifestar Pharma LLC70756-050
Midodrine HydrochlorideMidodrine hydrochloride 2.5 mg/1TabletOralMajor Pharmaceuticals0904-7640
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralMajor Pharmaceuticals0904-7641
Midodrine HydrochlorideMidodrine hydrochloride 10 mg/1TabletOralMajor Pharmaceuticals0904-7642

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