What is NDC 82619-135?

82619-135 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 160 mg/1 capsule, extended release, listed with the FDA by Creekwood Pharmaceuticals LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Creekwood Pharmaceuticals LLC, NDC labeler code 82619. 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 82619-135

NDC codes

FDA NDC Directory

Product NDC (as listed)82619-135Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82619-0135Add 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	Copy
82619-135-01	8261901350182619013501	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82619-135-01)Marketed from Aug 29, 2026
82619-135-02	8261901350282619013502	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82619-135-02)Marketed from Aug 29, 2026

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 — 160 mg/1
Dosage form: Capsule, Extended release
Route: Oral
Labeler: Creekwood Pharmaceuticals LLCNDC labeler code 82619
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219460
Marketing start: Aug 29, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 82619-135_598d91b8-2d91-47e7-e063-6294a90a248aSPL ID 598d91b8-2d91-47e7-e063-6294a90a248aSPL set ID 289f39f4-ebd3-4fd9-bbb3-72de8124795aRxCUI 856460, 856481, 856535, 856569UNII F8A3652H1VUPC 0382619134018, 0382619135015, 0382619132014, 0382619133011
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

N482619013501 followed by a unit qualifier and the quantity

Package 82619-0135-01. 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 Aug 21, 2026.

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 82619-135

What is NDC 82619-135?: 82619-135 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 160 mg/1 capsule, extended release, listed with the FDA by Creekwood Pharmaceuticals LLC. It has 2 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?: Creekwood Pharmaceuticals LLC, NDC labeler code 82619. 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 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
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Coupler LLC	67046-0211	67046-0211-03

All 197 Propranolol Hydrochloride NDCs

Other NDCs under ANDA 219460

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

FDA NDC Directory listings under ANDA 219460
Product	Strength	Form · route	Labeler	Product NDC
Propranolol Hydrochloride	Propranolol hydrochloride 60 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-132
Propranolol Hydrochloride	Propranolol hydrochloride 80 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-133
Propranolol Hydrochloride	Propranolol hydrochloride 120 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-134