Over-the-counter drug · ANDA
Naproxen Sodium BACK AND MUSCLE PAIN NDC 58602-736
naproxen sodium · Naproxen sodium 220 mg/1 · Tablet, Film coated · Oral · Aurohealth LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 58602-736-07 | 58602073607 | 1 BOTTLE in 1 CARTON (58602-736-07) / 24 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021 | |
| 58602-736-19 | 58602073619 | 1 BOTTLE in 1 CARTON (58602-736-19) / 90 TABLET, FILM COATED in 1 BOTTLEMarketed from Sep 21, 2023 | |
| 58602-736-21 | 58602073621 | 1 BOTTLE in 1 CARTON (58602-736-21) / 100 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021 | |
| 58602-736-29 | 58602073629 | 1 BOTTLE in 1 CARTON (58602-736-29) / 150 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021 | |
| 58602-736-38 | 58602073638 | 1 BOTTLE in 1 CARTON (58602-736-38) / 300 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021 | |
| 58602-736-40 | 58602073640 | 1 BOTTLE in 1 CARTON (58602-736-40) / 500 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021 | |
| 58602-736-78 | 58602073678 | 1 BOTTLE in 1 CARTON (58602-736-78) / 50 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021 |
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 BACK AND MUSCLE PAIN
- Generic name (nonproprietary)
- naproxen sodium
- Active ingredients
- Naproxen sodium — 220 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Aurohealth LLC
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 205497
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 58602-736_c640a53f-e070-4393-ba97-21c4c7c526e5SPL ID c640a53f-e070-4393-ba97-21c4c7c526e5SPL set ID c2066fce-cfa2-426d-ab6d-1a426736612bRxCUI 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
N458602073607followed by a unit qualifier and the quantityPackage 58602-0736-07. 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: backache muscular aches minor pain of arthritis menstrual cramps headache toothache the common cold temporarily reduces fever
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 205497
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 HEADACHE PAINnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-737 |
| Naproxen Sodium HEADACHE PAINnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-735 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-738 |
| Naproxen Sodium BACK AND MUSCLE PAINnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-739 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-819 |
| Amazon Basic Care Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-366 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-845 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | WALMART INC. | 79903-232 |
| Flanax Pain Reliever/Fever Reducernaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Belmora LLC | 27854-700 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | WALMART INC. | 79903-231 |
| Ana-Dent PAIN RELIEFnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Belmora LLC | 27854-701 |
- openFDA data updated
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Reference information only. Verify codes and billing rules against the applicable payer and official source before submitting a claim. How Med-Code handles data.