Over-the-counter drug · ANDA
All Day Back and Muscle Pain Relief (Naproxen sodium) NDC 79903-609
Naproxen sodium 220 mg/1 · Tablet, Coated · Oral · Walmart Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 79903-609-09 | 7990306090979903060909 | 1 BOTTLE in 1 CARTON (79903-609-09) / 90 TABLET, COATED in 1 BOTTLEMarketed from Dec 15, 2023 | |
| 79903-609-20 | 7990306092079903060920 | 1 BOTTLE in 1 CARTON (79903-609-20) / 200 TABLET, COATED in 1 BOTTLEMarketed from Dec 15, 2023 |
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)
- All Day Back and Muscle Pain Relief
- Generic name (nonproprietary)
- naproxen sodium
- Active ingredients
- Naproxen sodium — 220 mg/1
- Dosage form
- Tablet, Coated
- Route
- Oral
- Labeler
- Walmart Inc.NDC labeler code 79903
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090545
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 79903-609_0bafa4ac-8c2d-006b-e063-6294a90ab1fcSPL ID 0bafa4ac-8c2d-006b-e063-6294a90ab1fcSPL set ID 062b9ffe-b4fc-9f5a-e063-6294a90a560eRxCUI 849574UNII 9TN87S3A3CUPC 0194346189106, 0194346189113
- 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
N479903060909followed by a unit qualifier and the quantityPackage 79903-0609-09. 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 79903-609
- What is NDC 79903-609?
- 79903-609 is the product NDC for All Day Back and Muscle Pain Relief, Naproxen sodium 220 mg/1 tablet, coated, listed with the FDA by Walmart Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- All Day Back and Muscle Pain Relief (Naproxen sodium).
- What is the active ingredient?
- Naproxen sodium.
- Who is the labeler?
- Walmart Inc., NDC labeler code 79903. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for All Day Back and Muscle Pain Relief?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Other NDCs under ANDA 090545
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 |
|---|---|---|---|---|
| Naproxen Sodium 220mg | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Grocery Outlet | 85828-394 |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | WALGREENS | 0363-6099 |
| Naproxen Sodiumnaproxen sodium, coated tablets | Naproxen sodium 220 mg/1 | TabletOral | MARKSANS PHARMA LIMITED | 25000-141 |
| Naproxen Sodiumnaproxen sodium tablet, coated | Naproxen sodium 220 mg/1 | TabletOral | MARKSANS PHARMA LIMITED | 25000-144 |
| Calmadol Pain Relievernaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | GRANDALL DISTRIBUTING, LLC | 48201-007 |
| Naproxen Caplets All day relief for painnaproxen sodium 220 mg | Naproxen sodium 220 mg/1 | TabletOral | Allegiant Health | 69168-362 |
| Flanax Pain Reliever/Fever Reducernaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Navajo Manufacturing Company Inc. | 67751-125 |
| Naproxen Sodium 220mg | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Allegiant Health | 69168-395 |
| Naproxen Capletsnaproxen sodium 220 mg | Naproxen sodium 220 mg/1 | TabletOral | Allegiant Health | 69168-394 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Kroger Company | 41226-609 |
| Flanax Pain Reliever/Fever reducernaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Belmora LLC | 27854-505 |
| Belmora Flanaxnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Belmora LLC | 27854-555 |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Walmart Inc. | 79903-389 |
| Naproxen Sodium 220mg | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Command Brands, LLC | 69197-394 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | TIME CAP LABORATORIES, INC | 49483-608 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | TIME CAP LABORATORIES, INC | 49483-609 |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | WALGREENS | 0363-9608 |
| Back And Muscle Painnaproxen | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | WALGREENS | 0363-9609 |
| Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | BETTER LIVING BRANDS, LLC | 21130-608 |
| Naproxen Sodium 220mg | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Athlete's Needs, Inc. | 53185-394 |
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