Prescription drug · ANDA

Propranolol Hydrochloride NDC 83980-006

Propranolol hydrochloride 20 mg/1 · Tablet · Oral · Ipca Laboratories Limited

NDC codes

FDA NDC Directory
Product NDC (as listed)83980-006Labeler and product segments. Claims need a package NDC.
Product NDC at billing width83980-0006Add 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
83980-006-0183980000601100 TABLET in 1 BOTTLE (83980-006-01)Marketed from Sep 19, 2024
83980-006-0583980000605500 TABLET in 1 BOTTLE (83980-006-05)Marketed from Sep 19, 2024
83980-006-10839800006101000 TABLET in 1 BOTTLE (83980-006-10)Marketed from Sep 19, 2024
83980-006-138398000061330 TABLET in 1 BOTTLE (83980-006-13)Marketed from Sep 19, 2024

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 — 20 mg/1
Dosage form
Tablet
Route
Oral
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 83980-006_7854dd0a-2a35-4d7f-afe4-210b28966928SPL ID 7854dd0a-2a35-4d7f-afe4-210b28966928SPL set ID 9288191e-4d07-4e37-ab66-7b9de9321cf3RxCUI 856448, 856457, 856519, 856556, 856578UNII F8A3652H1VUPC 0383980005013, 0383980008014, 0383980009011, 0383980007017, 0383980006010
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

N483980000601 followed by a unit qualifier and the quantity

Package 83980-0006-01. 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)

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 40 mg/1TabletOralA-S Medication Solutions50090-7618
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralREMEDYREPACK INC.70518-4454
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralA-S Medication Solutions50090-7620
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralBryant Ranch Prepack71335-3097
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralREMEDYREPACK INC.70518-4471
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-3117
Propranolol HCLPropranolol hydrochloride 10 mg/1TabletOralDirect_Rx72189-672
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralAmerican Health Packaging60687-926
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralAmerican Health Packaging60687-937
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralAmerican Health Packaging60687-948
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralIpca Laboratories Limited83980-005
Propranolol HydrochloridePropranolol hydrochloride 80 mg/1TabletOralIpca Laboratories Limited83980-009
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralIpca Laboratories Limited83980-007
Propranolol HydrochloridePropranolol hydrochloride 60 mg/1TabletOralIpca Laboratories Limited83980-008
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4089
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralBryant Ranch Prepack71335-3137
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0583
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-5321
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralProficient Rx LP82804-258
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralProficient Rx LP82804-284

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Propranolol Hydrochloride NDC 83980-006 | Med-Code