Over-the-counter drug · ANDA
rugby all day relief (Naproxen sodium) NDC 0536-1094
Naproxen sodium 220 mg/1 · Tablet, Film coated · Oral · Rugby Laboratories
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0536-1094-06 | 00536109406 | 1 BOTTLE in 1 CARTON (0536-1094-06) / 50 TABLET, FILM COATED in 1 BOTTLEMarketed from Sep 2, 2015 | |
| 0536-1094-11 | 00536109411 | 1 BOTTLE in 1 CARTON (0536-1094-11) / 90 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 27, 2022 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
- rugby all day relief
- Generic name (nonproprietary)
- naproxen sodium
- Active ingredients
- Naproxen sodium — 220 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Rugby LaboratoriesNDC labeler code 0536
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 074661
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 0536-1094_d7f82128-5f85-4af6-9ba8-4279725ca3efSPL ID d7f82128-5f85-4af6-9ba8-4279725ca3efSPL set ID f587a428-291c-4c54-80fe-244a961b0521RxCUI 849574UNII 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
N400536109406followed by a unit qualifier and the quantityPackage 00536-1094-06. 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: • 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.
About NDC 0536-1094
- What is NDC 0536-1094?
- 0536-1094 is the product NDC for rugby all day relief (naproxen sodium), Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by Rugby Laboratories. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- rugby all day relief (Naproxen Sodium).
- What is the active ingredient?
- Naproxen sodium.
- Who is the labeler?
- Rugby Laboratories, NDC labeler code 0536. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for rugby all day relief?
- 3 other product NDCs are listed under this name. See all rugby all day relief NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other rugby all day relief products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Rugby All Day Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Rugby Laboratories | 0536-1093 | 00536-1093-0600536-1093-11 |
| rugby all day reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-3356 | 50090-3356-0050090-3356-01 |
| Rugby All Day Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-3009 | 71335-3009-0171335-3009-0271335-3009-03+6 more |
Other NDCs under ANDA 074661
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 |
|---|---|---|---|---|
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Walgreen Company | 0363-0368 |
| all day pain reliefnaproxen sodium | Naproxen sodium 200 mg/1 | Tablet, Film coatedOral | Walgreen Company | 0363-0938 |
| All Day Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Publix Super Markets Inc | 56062-368 |
| all day reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Publix Super Markets Inc | 56062-490 |
| Basic Care Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-331 |
| basic care naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-368 |
| Basic Care Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-489 |
| Berkley and Jensen Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | BJWC | 68391-368 |
| betr headache pain reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Live Betr LLC | 80267-001 |
| Care One Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | American Sales Company | 41520-349 |
| Care One Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | American Sales Company | 41520-533 |
| CareOne Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | American Sales Company | 41520-507 |
| DG Health Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Dolgencorp Inc | 55910-481 |
| DG Health Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Dolgencorp Inc | 55910-490 |
| dg health naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Dolgencorp Inc | 55910-500 |
| dg health naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Dolgencorp Inc | 55910-729 |
| equaline naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | United Natural Foods, Inc. dba UNFI | 41163-511 |
| equaline naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | United Natural Foods, Inc. dba UNFI | 41163-707 |
| exchange select naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Army & Air Force Exchange Service | 55301-368 |
| foster and thrive all day pain reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Strategic Sourcing Services LLC | 70677-1137 |
Showing 20 of 40.