What is NDC 51407-237?

51407-237 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 40 mg/1 tablet, listed with the FDA by Golden State Medical Supply, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Golden State Medical Supply, Inc., NDC labeler code 51407. 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 51407-237

NDC codes

FDA NDC Directory

Product NDC (as listed)51407-237Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51407-0237Add 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
51407-237-01	5140702370151407023701	100 TABLET in 1 BOTTLE, PLASTIC (51407-237-01)Marketed from May 15, 2019
51407-237-10	5140702371051407023710	1000 TABLET in 1 BOTTLE, PLASTIC (51407-237-10)Marketed from May 15, 2019

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: Golden State Medical Supply, Inc.NDC labeler code 51407
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 070213
Marketing start: Nov 19, 1985
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 51407-237_4f863b93-23da-bc07-e063-6394a90aed3bSPL ID 4f863b93-23da-bc07-e063-6394a90aed3bSPL set ID 8cbac6dc-ef1d-6662-e053-2995a90af13fRxCUI 856448, 856457, 856519, 856556, 856578UNII 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

N451407023701 followed by a unit qualifier and the quantity

Package 51407-0237-01. 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 Apr 15, 2026.

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 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. Myocardial …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51407-237

What is NDC 51407-237?: 51407-237 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 40 mg/1 tablet, listed with the FDA by Golden State Medical Supply, Inc.. 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?: Golden State Medical Supply, Inc., NDC labeler code 51407. 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 070213

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

FDA NDC Directory listings under ANDA 070213
Product	Strength	Form · route	Labeler	Product NDC
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Mylan Pharmaceuticals Inc.	0378-0182
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Mylan Pharmaceuticals Inc.	0378-0183
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	Mylan Pharmaceuticals Inc.	0378-0184
Propranolol Hydrochloride	Propranolol hydrochloride 80 mg/1	TabletOral	Mylan Pharmaceuticals Inc.	0378-0185
Propranolol Hydrochloride	Propranolol hydrochloride 60 mg/1	TabletOral	Mylan Pharmaceuticals Inc.	0378-0187
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	43353-961
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-235
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-236
Propranolol Hydrochloride	Propranolol hydrochloride 80 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-238
Propranolol Hydrochloride	Propranolol hydrochloride 60 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-239
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-339