What is NDC 68788-7800?

68788-7800 is the product NDC for Naproxen Sodium, Naproxen sodium 550 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals, Inc.. It has 7 package NDCs, shown above in 10- and 11-digit form.

Preferred Pharmaceuticals, Inc., NDC labeler code 68788. 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 68788-7800 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-7800Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-7800Add 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
68788-7800-1	6878878000168788780001	100 TABLET in 1 BOTTLE (68788-7800-1)Marketed from Oct 13, 2020
68788-7800-2	6878878000268788780002	20 TABLET in 1 BOTTLE (68788-7800-2)Marketed from Oct 13, 2020
68788-7800-3	6878878000368788780003	30 TABLET in 1 BOTTLE (68788-7800-3)Marketed from Oct 13, 2020
68788-7800-4	6878878000468788780004	14 TABLET in 1 BOTTLE (68788-7800-4)Marketed from Oct 13, 2020
68788-7800-6	6878878000668788780006	60 TABLET in 1 BOTTLE (68788-7800-6)Marketed from Oct 13, 2020
68788-7800-8	6878878000868788780008	120 TABLET in 1 BOTTLE (68788-7800-8)Marketed from Oct 13, 2020
68788-7800-9	6878878000968788780009	90 TABLET in 1 BOTTLE (68788-7800-9)Marketed from Oct 13, 2020

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 550 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Preferred Pharmaceuticals, Inc.NDC labeler code 68788
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212199
Marketing start: Oct 13, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 68788-7800_e522f024-b4ac-4ff4-8368-e9e6da9eb37eSPL ID e522f024-b4ac-4ff4-8368-e9e6da9eb37eSPL set ID 6ae413ba-5a48-423f-8b8d-7a42661cf836RxCUI 849431UNII 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

N468788780001 followed by a unit qualifier and the quantity

Package 68788-7800-01. 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 18, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Naproxen sodium tablets are non-steroidal anti-inflammatory drugs indicated for: the relief of the signs and symptoms of: • rheumatoid arthritis • osteoarthritis • ankylosing spondylitis • polyarticular juvenile idiopathic arthritis Naproxen sodium tablets are also indicated for: the relief of the signs and symptoms of: • tendonitis • bursitis • acute gout the management of: • pain • primary dysmenorrhea Naproxen sodium tablets are non-steroidal anti-inflammatory drugs indicated for: the relief of the signs and symptoms of: • rheumatoid arthritis • osteoarthritis • ankylosing spondylitis • polyarticular juvenile idiopathic arthritis Naproxen sodium tablets are also indicated for: the relief …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-7800

What is NDC 68788-7800?: 68788-7800 is the product NDC for Naproxen Sodium, Naproxen sodium 550 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals, Inc.. It has 7 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?: Preferred Pharmaceuticals, Inc., NDC labeler code 68788. 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 212199

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

FDA NDC Directory listings under ANDA 212199
Product	Strength	Form · route	Labeler	Product NDC
Naproxen Sodium	Naproxen sodium 275 mg/1	TabletOral	Asclemed USA, Inc.	76420-637
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Asclemed USA, Inc.	76420-627
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Bryant Ranch Prepack	71335-2294
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Direct Rx	72189-332
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Bryant Ranch Prepack	63629-8516
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Bryant Ranch Prepack	63629-8517
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Proficient Rx LP	71205-631
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-801
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0531
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-2333
Naproxen Sodium	Naproxen sodium 275 mg/1	TabletOral	ScieGen Pharmaceuticals, Inc.	50228-432
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0574
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	ScieGen Pharmaceuticals, Inc.	50228-433
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-389
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Bryant Ranch Prepack	71335-9663