Prescription drug · ANDA

Propranolol Hydrochloride NDC 0904-7468

Propranolol hydrochloride 20 mg/1 · Tablet · Oral · Major Pharmaceuticals

NDC codes

FDA NDC Directory
Product NDC (as listed)0904-7468Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00904-7468Add 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
0904-7468-060090474680650 BLISTER PACK in 1 CARTON (0904-7468-06) / 1 TABLET in 1 BLISTER PACKMarketed from Sep 20, 2024
0904-7468-6100904746861100 BLISTER PACK in 1 CARTON (0904-7468-61) / 1 TABLET in 1 BLISTER PACKMarketed from Sep 20, 2024

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 20 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 071972
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 0904-7468_eba5a266-7acd-4a0b-b1ce-61c313bae40eSPL ID eba5a266-7acd-4a0b-b1ce-61c313bae40eSPL set ID e7218c9b-b9b8-4cf0-a2c7-c759ad3a65baRxCUI 856448, 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

N400904746806 followed by a unit qualifier and the quantity

Package 00904-7468-06. 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. It may be used alone or used in combination with other antihypertensive agents, particularly a thiazide diuretic. Propranolol hydrochloride is 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. Myocardial Infarctio…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 071972

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

FDA NDC Directory listings under ANDA 071972
ProductStrengthForm · routeLabelerProduct NDC
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralCoupler LLC67046-0211
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralBryant Ranch Prepack71335-2369
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralBryant Ranch Prepack71335-2371
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-2372
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0463
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-731
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralNorthwind Health Company, LLC82868-003
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralA-S Medication Solutions50090-7097
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralA-S Medication Solutions50090-7101
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralA-S Medication Solutions50090-7104
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralREMEDYREPACK INC.70518-3281
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8595
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralAvPAK50268-662
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralAvPAK50268-663
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralAvPAK50268-664
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8604
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-372
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralREMEDYREPACK INC.70518-3377
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralNorthwind Health Company, LLC51655-228
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralMajor Pharmaceuticals0904-7467

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Propranolol Hydrochloride NDC 0904-7468 | Med-Code