What is NDC 81469-141?

81469-141 is the product NDC for Midodrine Hydrochloride, Midodrine hydrochloride 10 mg/1 tablet, listed with the FDA by First Nation Group, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

First Nation Group, LLC, NDC labeler code 81469. 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 81469-141

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 NDC	11-digit (billing)	Package	Copy
81469-141-90	8146901419081469014190	90 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
Labeler: First Nation Group, LLCNDC labeler code 81469
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217271
Marketing start: Aug 13, 2025
Listing expires: Dec 31, 2026
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 Aug 13, 2025. 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)

About NDC 81469-141

What is NDC 81469-141?: 81469-141 is the product NDC for Midodrine Hydrochloride, Midodrine hydrochloride 10 mg/1 tablet, listed with the FDA by First Nation Group, 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?: First Nation Group, LLC, NDC labeler code 81469. 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 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
Product	Strength	Form · route	Labeler	Product NDC
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	Major Pharmaceuticals	0904-7640
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	Major Pharmaceuticals	0904-7641
Midodrine Hydrochloride	Midodrine hydrochloride 10 mg/1	TabletOral	Major Pharmaceuticals	0904-7642
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	Coupler LLC	67046-1512
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	Lifestar Pharma LLC	70756-010
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	Lifestar Pharma LLC	70756-049
Midodrine Hydrochloride	Midodrine hydrochloride 10 mg/1	TabletOral	Lifestar Pharma LLC	70756-050
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	NorthStar RxLLC	72603-906
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	NorthStar RxLLC	72603-907
Midodrine Hydrochloride	Midodrine hydrochloride 10 mg/1	TabletOral	NorthStar RxLLC	72603-908
Midodrine Hydrochloride	Midodrine hydrochloride 2.5 mg/1	TabletOral	First Nation Group, LLC	81469-139
Midodrine Hydrochloride	Midodrine hydrochloride 5 mg/1	TabletOral	First Nation Group, LLC	81469-140