Prescription drug · ANDA

Midodrine Hydrochloride NDC 71205-906

Midodrine hydrochloride 10 mg/1 · Tablet · Oral · Proficient Rx LP

NDC codes

FDA NDC Directory
Product NDC (as listed)71205-906Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0906Add 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
71205-906-0071205090600100 TABLET in 1 BOTTLE, PLASTIC (71205-906-00)Marketed from Jul 20, 2021
71205-906-11712050906111000 TABLET in 1 BOTTLE, PLASTIC (71205-906-11)Marketed from Jul 20, 2021
71205-906-307120509063030 TABLET in 1 BOTTLE, PLASTIC (71205-906-30)Marketed from Jul 20, 2021
71205-906-5571205090655500 TABLET in 1 BOTTLE, PLASTIC (71205-906-55)Marketed from Jul 20, 2021
71205-906-607120509066060 TABLET in 1 BOTTLE, PLASTIC (71205-906-60)Marketed from Jul 20, 2021
71205-906-7271205090672120 TABLET in 1 BOTTLE, PLASTIC (71205-906-72)Marketed from Jul 20, 2021
71205-906-907120509069090 TABLET in 1 BOTTLE, PLASTIC (71205-906-90)Marketed from Jul 20, 2021

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 207849
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)
Identifiers
Product ID 71205-906_fac1a712-e714-4137-8604-2ba0f048901cSPL ID fac1a712-e714-4137-8604-2ba0f048901cSPL set ID 0aebf5f9-8cfa-4b77-ba40-821ce0a2b266RxCUI 993462, 993466, 993470UNII 59JV96YTXVUPC 0371205906306, 0371205905309, 0371205904302
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

N471205090600 followed by a unit qualifier and the quantity

Package 71205-0906-00. 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' 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 o…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 207849

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

FDA NDC Directory listings under ANDA 207849
ProductStrengthForm · routeLabelerProduct NDC
Midodrine HydrochlorideMidodrine hydrochloride 2.5 mg/1TabletOralProficient Rx LP71205-904
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralProficient Rx LP71205-905
Midodrine HydrochlorideMidodrine hydrochloride 10 mg/1TabletOralBryant Ranch Prepack63629-2346
Midodrine HydrochlorideMidodrine hydrochloride 2.5 mg/1TabletOralXiromed, LLC70700-157
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralBryant Ranch Prepack63629-2347
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralXiromed, LLC70700-158
Midodrine HydrochlorideMidodrine hydrochloride 2.5 mg/1TabletOralBryant Ranch Prepack63629-2348
Midodrine HydrochlorideMidodrine hydrochloride 10 mg/1TabletOralXiromed, LLC70700-159
Midodrine HydrochlorideMidodrine hydrochloride 2.5 mg/1TabletOralBryant Ranch Prepack72162-1973
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralBryant Ranch Prepack72162-1974
Midodrine HydrochlorideMidodrine hydrochloride 10 mg/1TabletOralBryant Ranch Prepack72162-1975
Midodrine HydrochlorideMidodrine hydrochloride 2.5 mg/1TabletOralGolden State Medical Supply, Inc.51407-388
Midodrine HydrochlorideMidodrine hydrochloride 5 mg/1TabletOralGolden State Medical Supply, Inc.51407-389
Midodrine HydrochlorideMidodrine hydrochloride 10 mg/1TabletOralGolden State Medical Supply, Inc.51407-390

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Midodrine Hydrochloride NDC 71205-906 | Med-Code