Prescription drug · ANDA

Propranolol Hydrochloride NDC 68788-4089

Propranolol hydrochloride 20 mg/1 · Tablet · Oral · Preferred Pharmaceuticals Inc.

NDC codes

FDA NDC Directory
Product NDC (as listed)68788-4089Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-4089Add 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
68788-4089-16878840890168788408901100 TABLET in 1 BOTTLE (68788-4089-1)Marketed from Mar 17, 2026

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 — 20 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078955
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 68788-4089_8bdb15bc-5a25-4f20-af98-79bcd26022b8SPL ID 8bdb15bc-5a25-4f20-af98-79bcd26022b8SPL set ID 8bdb15bc-5a25-4f20-af98-79bcd26022b8RxCUI 856457UNII 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

N468788408901 followed by a unit qualifier and the quantity

Package 68788-4089-01. 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 tablets are indicated in the management of hypertension. They may be used alone or used in combination with other antihypertensive agents, particularly a thiazide diuretic. Propranolol hydrochloride tablets are not indicated in the management of hypertensive emergencies. Angina Pectoris Due to Coronary Atherosclerosis Propranolol hydrochloride tablets are indicated to decrease angina frequency and increase exercise tolerance in patients with angina pectoris. Atrial Fibrillation Propranolol hydrochloride tablets are indicated to control ventricular rate in patients with atrial fibrillation and a rapid ventricular response. Myocardia…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-4089

What is NDC 68788-4089?
68788-4089 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 20 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 1 package NDC, 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?
Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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 078955

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

FDA NDC Directory listings under ANDA 078955
ProductStrengthForm · routeLabelerProduct NDC
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralProficient Rx LP82804-284
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralCardinal Health 107, LLC55154-2584
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralREMEDYREPACK INC.70518-4454
Propranolol HydrochloridePropranolol hydrochloride 60 mg/1TabletOralIpca Laboratories Limited83980-008
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralIpca Laboratories Limited83980-005
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralIpca Laboratories Limited83980-006
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralIpca Laboratories Limited83980-007
Propranolol HydrochloridePropranolol hydrochloride 80 mg/1TabletOralIpca Laboratories Limited83980-009
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralBryant Ranch Prepack71335-3097
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralAmerican Health Packaging60687-926
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralAmerican Health Packaging60687-937
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-3117
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralAmerican Health Packaging60687-948
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralBryant Ranch Prepack71335-3137
Propranolol HCLPropranolol hydrochloride 10 mg/1TabletOralDirect_Rx72189-672
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralREMEDYREPACK INC.70518-4471
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-5321
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0583
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralA-S Medication Solutions50090-7593
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4131

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