Over-the-counter drug · ANDA
Amazon Basic Care Naproxen Sodium NDC 72288-366
naproxen sodium · Naproxen sodium 220 mg/1 · Tablet, Film coated · Oral · Amazon.com Services LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72288-366-20 | 72288036620 | 1 BOTTLE in 1 CARTON (72288-366-20) / 200 TABLET, FILM COATED in 1 BOTTLEMarketed from May 15, 2024 | |
| 72288-366-30 | 72288036630 | 1 BOTTLE in 1 CARTON (72288-366-30) / 300 TABLET, FILM COATED in 1 BOTTLEMarketed from May 15, 2024 | |
| 72288-366-90 | 72288036690 | 1 BOTTLE in 1 CARTON (72288-366-90) / 90 TABLET, FILM COATED in 1 BOTTLEMarketed from May 15, 2024 |
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)
- Amazon Basic Care Naproxen Sodium
- Generic name (nonproprietary)
- naproxen sodium
- Active ingredients
- Naproxen sodium — 220 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Amazon.com Services 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 72288-366_0931d3d1-7ac4-4076-865e-a8ba9e295bc8SPL ID 0931d3d1-7ac4-4076-865e-a8ba9e295bc8SPL set ID 10ee5bc0-509d-b549-e063-6394a90a5dcaRxCUI 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
N472288036620followed by a unit qualifier and the quantityPackage 72288-0366-20. 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 minor pain of arthritis muscular aches backache menstrual cramps 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 BACK AND MUSCLE PAINnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Aurohealth LLC | 58602-736 |
| 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 |
| 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.