What is NDC 83980-007?

83980-007 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 40 mg/1 tablet, listed with the FDA by Ipca Laboratories Limited. It has 4 package NDCs, shown above in 10- and 11-digit form.

Ipca Laboratories Limited, NDC labeler code 83980. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Propranolol Hydrochloride NDC 83980-007

NDC codes

FDA NDC Directory

Product NDC (as listed)83980-007Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83980-0007Add 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 NDC	11-digit (billing)	Package
83980-007-01	8398000070183980000701	100 TABLET in 1 BOTTLE (83980-007-01)Marketed from Sep 19, 2024
83980-007-05	8398000070583980000705	500 TABLET in 1 BOTTLE (83980-007-05)Marketed from Sep 19, 2024
83980-007-10	8398000071083980000710	1000 TABLET in 1 BOTTLE (83980-007-10)Marketed from Sep 19, 2024
83980-007-13	8398000071383980000713	30 TABLET in 1 BOTTLE (83980-007-13)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 — 40 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Ipca Laboratories LimitedNDC labeler code 83980
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078955
Marketing start: Sep 19, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 83980-007_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

N483980000701 followed by a unit qualifier and the quantity

Package 83980-0007-01. 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 Dec 17, 2025.

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 83980-007

What is NDC 83980-007?: 83980-007 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 40 mg/1 tablet, listed with the FDA by Ipca Laboratories Limited. It has 4 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?: Ipca Laboratories Limited, NDC labeler code 83980. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	American Health Packaging	60687-948	60687-0948-01
Propranolol Hydrochloride	Propranolol hydrochloride 60 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-132	82619-0132-0182619-0132-02
Propranolol Hydrochloride	Propranolol hydrochloride 80 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-133	82619-0133-0182619-0133-02
Propranolol Hydrochloride	Propranolol hydrochloride 120 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-134	82619-0134-0182619-0134-02
Propranolol Hydrochloride	Propranolol hydrochloride 160 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-135	82619-0135-0182619-0135-02
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-0958	00121-0958-16
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-4958	00121-4958-40
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2584	55154-2584-00
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	American Health Packaging	60687-937	60687-0937-01
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0583	80425-0583-0180425-0583-0280425-0583-03

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
Product	Strength	Form · route	Labeler	Product NDC
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Proficient Rx LP	82804-284
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2584
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4454
Propranolol Hydrochloride	Propranolol hydrochloride 60 mg/1	TabletOral	Ipca Laboratories Limited	83980-008
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Ipca Laboratories Limited	83980-005
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Ipca Laboratories Limited	83980-006
Propranolol Hydrochloride	Propranolol hydrochloride 80 mg/1	TabletOral	Ipca Laboratories Limited	83980-009
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-3097
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	American Health Packaging	60687-926
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	American Health Packaging	60687-937
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-3117
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	American Health Packaging	60687-948
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	Bryant Ranch Prepack	71335-3137
Propranolol HCL	Propranolol hydrochloride 10 mg/1	TabletOral	Direct_Rx	72189-672
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4471
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4089
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-5321
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0583
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	A-S Medication Solutions	50090-7593
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4131

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