NDC codes

FDA NDC Directory
Product NDC (as listed)53401-039Labeler and product segments. Claims need a package NDC.
Product NDC at billing width53401-0039Add 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
53401-039-53534010039535340100395360 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53401-039-53)Marketed from Sep 21, 2026
53401-039-60534010039605340100396090 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53401-039-60)Marketed from Sep 21, 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)
Propranolol Hydrochloride
Generic name (nonproprietary)
propranolol hydrochloride
Active ingredients
Propranolol hydrochloride — 60 mg/1
Dosage form
Capsule, Extended release
Route
Oral
Labeler
Aphena Pharma Solutions - Tennessee, LLCNDC labeler code 53401
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212026
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 53401-039_5c008ef7-bf45-f11a-e063-6394a90ae1e1SPL ID 5c008ef7-bf45-f11a-e063-6394a90ae1e1
Pharmacologic class
beta-Adrenergic Blocker

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

N453401003953 followed by a unit qualifier and the quantity

Package 53401-0039-53. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 53401-039

What is NDC 53401-039?
53401-039 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 60 mg/1 capsule, extended release, listed with the FDA by Aphena Pharma Solutions - Tennessee, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Propranolol Hydrochloride.
What is the active ingredient?
Propranolol hydrochloride.
Who is the labeler?
Aphena Pharma Solutions - Tennessee, LLC, NDC labeler code 53401. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Propranolol Hydrochloride?
196 other product NDCs are listed under this name. See all Propranolol 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 Propranolol Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralAmerican Health Packaging60687-94860687-0948-01
Propranolol HydrochloridePropranolol hydrochloride 60 mg/1Capsule, Extended releaseOralCreekwood Pharmaceuticals LLC82619-13282619-0132-0182619-0132-02
Propranolol HydrochloridePropranolol hydrochloride 80 mg/1Capsule, Extended releaseOralCreekwood Pharmaceuticals LLC82619-13382619-0133-0182619-0133-02
Propranolol HydrochloridePropranolol hydrochloride 120 mg/1Capsule, Extended releaseOralCreekwood Pharmaceuticals LLC82619-13482619-0134-0182619-0134-02
Propranolol HydrochloridePropranolol hydrochloride 160 mg/1Capsule, Extended releaseOralCreekwood Pharmaceuticals LLC82619-13582619-0135-0182619-0135-02
Propranolol HydrochloridePropranolol hydrochloride 20 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-095800121-0958-16
Propranolol HydrochloridePropranolol hydrochloride 20 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-495800121-4958-40
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralCardinal Health 107, LLC55154-258455154-2584-00
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralAmerican Health Packaging60687-93760687-0937-01
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-058380425-0583-0180425-0583-0280425-0583-03

All 197 Propranolol Hydrochloride NDCs

Other NDCs under ANDA 212026

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

FDA NDC Directory listings under ANDA 212026
ProductStrengthForm · routeLabelerProduct NDC
Propranolol HCL ERPropranolol hydrochloride 60 mg/1Capsule, Extended releaseOralDirect_Rx72189-691
Propranolol HydrochloridePropranolol hydrochloride 60 mg/1Capsule, Extended releaseOralLannett Company, Inc.0527-4116
Propranolol HydrochloridePropranolol hydrochloride 80 mg/1Capsule, Extended releaseOralLannett Company, Inc.0527-4117
Propranolol HydrochloridePropranolol hydrochloride 120 mg/1Capsule, Extended releaseOralLannett Company, Inc.0527-4118
Propranolol HydrochloridePropranolol hydrochloride 160 mg/1Capsule, Extended releaseOralLannett Company, Inc.0527-4119
Propranolol HydrochloridePropranolol hydrochloride 80 mg/1Capsule, Extended releaseOralA-S Medication Solutions50090-7263
Propranolol HydrochloridePropranolol hydrochloride 80 mg/1Capsule, Extended releaseOralBryant Ranch Prepack63629-9953
Propranolol HydrochloridePropranolol hydrochloride 80 mg/1Capsule, Extended releaseOralREMEDYREPACK INC.70518-3552
Propranolol HydrochloridePropranolol hydrochloride 60 mg/1Capsule, Extended releaseOralBryant Ranch Prepack71335-1765

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