Over-the-counter drug · ANDA
Naproxen Sodium NDC 11822-6040
Naproxen sodium 220 mg/1 · Tablet, Film coated · Oral · Rite Aid Corporation
NDC codes
FDA NDC DirectoryProduct NDC (as listed)11822-6040Labeler and product segments. Claims need a package NDC.
Product NDC at billing width11822-6040Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 11822-6040-5 | 1182260400511822604005 | 1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-5) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Jul 18, 2022 | |
| 11822-6040-6 | 1182260400611822604006 | 1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-6) / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Jul 18, 2022 | |
| 11822-6040-7 | 1182260400711822604007 | 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-6040-7)Marketed from Jul 18, 2022 | |
| 11822-6040-8 | 1182260400811822604008 | 1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-8) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Jul 18, 2022 | |
| 11822-6040-9 | 1182260400911822604009 | 1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-9) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Jul 18, 2022 |
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 — 220 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Rite Aid CorporationNDC labeler code 11822
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 204872
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 11822-6040_cade5181-be44-48b9-9c46-d29c48570efdSPL ID cade5181-be44-48b9-9c46-d29c48570efdSPL set ID e6277515-c606-4535-9c29-08cade045aeeRxCUI 849574UNII 9TN87S3A3CUPC 0011822420358
- 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
N411822604005followed by a unit qualifier and the quantityPackage 11822-6040-05. 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 .
Indications (excerpt from the label)
Uses temporarily relieves minor aches and pains due to: headache muscular aches the common cold toothache backache menstrual cramps minor pain of arthritis temporarily reduces fever
Excerpt only. Read the full label for complete information.
About NDC 11822-6040
- What is NDC 11822-6040?
- 11822-6040 is the product NDC for Naproxen Sodium, Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by Rite Aid Corporation. It has 5 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?
- Rite Aid Corporation, NDC labeler code 11822. 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?
- 141 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.
Related NDCs: other Naproxen Sodium products
Other finished products listed under the same name: strengths, forms and labelers.
| 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 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 | 42507-0245-0142507-0245-14 |
| 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 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | CHAIN DRUG MARKETING ASSOCIATION, INC. | 83324-109 | 83324-0109-0183324-0109-50 |
Other NDCs under ANDA 204872
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-5039 |
| 24/7 Life by 7-Eleven Naproxen Sodiumnaproxen sodium tablet, film coated | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Lil' Drug Store Products, Inc. | 66715-5428 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1282 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Geri-Care Pharmaceutical Corp | 57896-954 |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | WALMART INC. | 79903-005 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Better Living Brands, LLC | 21130-856 |
| Back and Muscle Painnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 51316-817 |
| Artridolnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Zapotol Products Corp | 59428-604 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Proficient Rx LP | 71205-595 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | L.N.K. International, Inc. | 50844-261 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amerisource Bergen | 46122-564 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amerisource Bergen | 46122-562 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | L.N.K. International, Inc. | 50844-417 |
| Naproxen Headache Painnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | L.N.K. International, Inc. | 50844-471 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | L.N.K. International, Inc. | 50844-604 |
| Flanaxnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Belmora LLC | 27854-160 |
| Flanax Menstrual Pain Relievernaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Belmora LLC | 27854-165 |
| AnaDentnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Belmora LLC | 27854-170 |
| Naproxen Back and Muscle Painnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | L.N.K. International, Inc. | 50844-714 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Preferred Pharmaceuticals, Inc. | 68788-7572 |
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