NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1765Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1765Add 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
71335-1765-1713351765017133517650130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-1)Marketed from Jan 8, 2021
71335-1765-2713351765027133517650218 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-2)Marketed from Sep 6, 2024
71335-1765-3713351765037133517650390 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-3)Marketed from Sep 6, 2024
71335-1765-4713351765047133517650428 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-4)Marketed from Sep 6, 2024
71335-1765-5713351765057133517650560 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-5)Marketed from Sep 6, 2024
71335-1765-6713351765067133517650610 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-6)Marketed from Sep 6, 2024
71335-1765-77133517650771335176507100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-7)Marketed from Sep 6, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Bryant Ranch PrepackNDC labeler code 71335
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 71335-1765_ebc207a3-62f9-4f11-a790-8caf04a30feaSPL ID ebc207a3-62f9-4f11-a790-8caf04a30feaSPL set ID ea98fedc-c440-487e-b144-35a8a389a446RxCUI 856535UNII F8A3652H1V
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

N471335176501 followed by a unit qualifier and the quantity

Package 71335-1765-01. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE Hypertension Propranolol Hydrochloride Extended-Release Capsules are indicated in the management of hypertension. It may be used alone or used in combination with other antihypertensive agents, particularly a thiazide diuretic. Propranolol Hydrochloride Extended-Release Capsules are not indicated in the management of hypertensive emergencies. Angina Pectoris Due to Coronary Atherosclerosis Propranolol Hydrochloride Extended-Release Capsules are indicated to decrease angina frequency and increase exercise tolerance in patients with angina pectoris. Migraine Propranolol Hydrochloride Extended-Release Capsules are indicated for the prophylaxis of common migraine headache. …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1765

What is NDC 71335-1765?
71335-1765 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 60 mg/1 capsule, extended release, listed with the FDA by Bryant Ranch Prepack. It has 7 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?
Bryant Ranch Prepack, NDC labeler code 71335. 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 60 mg/1Capsule, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC53401-039
Propranolol HydrochloridePropranolol hydrochloride 80 mg/1Capsule, Extended releaseOralBryant Ranch Prepack63629-9953
Propranolol HydrochloridePropranolol hydrochloride 80 mg/1Capsule, Extended releaseOralREMEDYREPACK INC.70518-3552

Free account

Log in to keep searching

You’ve used your 3 free searches. Med-Code is free: log in or create a free profile to keep looking up NDCs, J-codes and drugs.

Create a free profileLog in