What is NDC 51013-137?

51013-137 is the product NDC for Naproxen Sodium, Naproxen sodium 220 mg/1 capsule, liquid filled, listed with the FDA by PuraCap Pharmaceutical LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.

PuraCap Pharmaceutical LLC, NDC labeler code 51013. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Naproxen Sodium?

144 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Naproxen Sodium NDC 51013-137 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51013-137Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51013-0137Add 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
51013-137-15	5101301371551013013715	1 BOTTLE in 1 CARTON (51013-137-15) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLEMarketed from Mar 20, 2018
51013-137-28	5101301372851013013728	1 BOTTLE in 1 CARTON (51013-137-28) / 160 CAPSULE, LIQUID FILLED in 1 BOTTLEMarketed from Mar 20, 2018
51013-137-60	5101301376051013013760	160 CAPSULE, LIQUID FILLED in 1 BOTTLE (51013-137-60)Marketed from Mar 20, 2018

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): Naproxen Sodium
Generic name (nonproprietary): naproxen sodium
Active ingredients: Naproxen sodium — 220 mg/1
Dosage form: Capsule, Liquid filled
Route: Oral
Labeler: PuraCap Pharmaceutical LLCNDC labeler code 51013
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208363
Marketing start: Mar 20, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 51013-137_9a223804-f229-442b-85a9-7f0f8fd74ba1SPL ID 9a223804-f229-442b-85a9-7f0f8fd74ba1SPL set ID fc865e81-164c-48e9-8fb9-6fc27d1c33cfRxCUI 1112231UNII 9TN87S3A3C
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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

N451013013715 followed by a unit qualifier and the quantity

Package 51013-0137-15. 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 10, 2019.

Indications (excerpt from the label)

Uses temporarily relieves minor aches and pains due to: minor pain of arthritis muscular aches backache menstrual cramps headache toothache the common cold temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51013-137

What is NDC 51013-137?: 51013-137 is the product NDC for Naproxen Sodium, Naproxen sodium 220 mg/1 capsule, liquid filled, listed with the FDA by PuraCap Pharmaceutical LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Naproxen Sodium.
What is the active ingredient?: Naproxen sodium.
Who is the labeler?: PuraCap Pharmaceutical LLC, NDC labeler code 51013. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Naproxen Sodium?: 144 other product NDCs are listed under this name. See all Naproxen Sodium 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 Naproxen Sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
naproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-988	72288-0988-75
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	AAA Pharmaceutical, Inc.	57344-244	57344-0244-03
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0574	80425-0574-0180425-0574-0280425-0574-03
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	HYVEE INC	42507-245	42507-0245-0142507-0245-0842507-0245-14
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	HYVEE INC	42507-844	42507-0844-0142507-0844-14
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	TARGET Corporation	11673-651	11673-0651-78
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Safeway	21130-593	21130-0593-79
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0531	80425-0531-0180425-0531-0280425-0531-03
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0532	80425-0532-0180425-0532-0280425-0532-03
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-108	83324-0108-0183324-0108-2483324-0108-50

All 145 Naproxen Sodium NDCs

Other NDCs under ANDA 208363

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

FDA NDC Directory listings under ANDA 208363
Product	Strength	Form · route	Labeler	Product NDC
All Day Reliefnaproxen sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	Publix Supermarkets, Inc.	56062-748
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	Walgreens	0363-0748
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	TARGET Corporation	11673-748
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	Safeway, Inc.	21130-748
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	Care One (American Sales Company)	41520-748
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)	49035-748
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	Humanwell PuraCap Pharmaceuticals (Wuhan) Co., Ltd	53345-042
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	AAFES/Your Military Exchanges	55301-748
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	55910-748
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	P & L Development, LLC	59726-174
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	CVS Pharmacy	69842-748
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	Strategic Sourcing Services LLC	70677-1148
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	Care One (Retail Business Services, LLC.)	72476-748