NDC codes

FDA NDC Directory
Product NDC (as listed)71610-339Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71610-0339Add 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
71610-339-457161003394545 TABLET in 1 BOTTLE, PLASTIC (71610-339-45)Marketed from May 7, 2021
71610-339-607161003396090 TABLET in 1 BOTTLE, PLASTIC (71610-339-60)Marketed from Aug 20, 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 — 20 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070213
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 71610-339_c8c0bd51-a7c2-4d89-bee2-063cd4da43f3SPL ID c8c0bd51-a7c2-4d89-bee2-063cd4da43f3SPL set ID 3c05ab1f-05b0-494a-b640-667e7cf517a1RxCUI 856457UNII 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

N471610033945 followed by a unit qualifier and the quantity

Package 71610-0339-45. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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
ProductStrengthForm · routeLabelerProduct NDC
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralGolden State Medical Supply, Inc.51407-235
Propranolol HydrochloridePropranolol hydrochloride 80 mg/1TabletOralGolden State Medical Supply, Inc.51407-238
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralGolden State Medical Supply, Inc.51407-236
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralGolden State Medical Supply, Inc.51407-237
Propranolol HydrochloridePropranolol hydrochloride 60 mg/1TabletOralGolden State Medical Supply, Inc.51407-239
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC43353-961
Propranolol HydrochloridePropranolol hydrochloride 10 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0182
Propranolol HydrochloridePropranolol hydrochloride 20 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0183
Propranolol HydrochloridePropranolol hydrochloride 40 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0184
Propranolol HydrochloridePropranolol hydrochloride 80 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0185
Propranolol HydrochloridePropranolol hydrochloride 60 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0187

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