What is NDC 0121-0958?

0121-0958 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 20 mg/5mL solution, listed with the FDA by PAI Holdings, LLC dba PAI Pharma. It has 1 package NDC, shown above in 10- and 11-digit form.

PAI Holdings, LLC dba PAI Pharma, NDC labeler code 0121. 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 0121-0958

NDC codes

FDA NDC Directory

Product NDC (as listed)0121-0958Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00121-0958Add 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
0121-0958-16	00121095816	500 mL in 1 BOTTLE (0121-0958-16)Marketed from Aug 19, 2026

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/5mL
Dosage form: Solution
Route: Oral
Labeler: PAI Holdings, LLC dba PAI PharmaNDC labeler code 0121
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219165
Marketing start: Aug 19, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 0121-0958_dc246a80-abe2-4ee7-b3c6-1ef93dad5e1dSPL ID dc246a80-abe2-4ee7-b3c6-1ef93dad5e1dSPL set ID fa5b6189-3419-4134-8bfe-c0d0c77df828RxCUI 856724UNII F8A3652H1VUPC 0301210958168
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

N400121095816 followed by a unit qualifier and the quantity

Package 00121-0958-16. 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 10, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hypertension Propranolol hydrochloride oral solution is 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 oral solution is not indicated in the management of hypertensive emergencies. Angina Pectoris Due to Coronary Atherosclerosis Propranolol hydrochloride oral solution is indicated to decrease angina frequency and increase exercise tolerance in patients with angina pectoris. Atrial Fibrillation Propranolol hydrochloride oral solution is indicated to control ventricular rate in patients with atrial fibrillation and a rapid ventricular r…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0121-0958

What is NDC 0121-0958?: 0121-0958 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 20 mg/5mL solution, listed with the FDA by PAI Holdings, LLC dba PAI Pharma. 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?: PAI Holdings, LLC dba PAI Pharma, NDC labeler code 0121. 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	0121-4958	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	Preferred Pharmaceuticals Inc.	68788-4131	68788-4131-01

All 197 Propranolol Hydrochloride NDCs

Other NDCs under ANDA 219165

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

FDA NDC Directory listings under ANDA 219165
Product	Strength	Form · route	Labeler	Product NDC
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-4958