Over-the-counter drug · ANDA
Dr Simi All Day Pain Relief (Naproxen sodium) NDC 85786-104
Naproxen sodium 220 mg/1 · Tablet, Film coated · Oral · Farmacias De Similares TX LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 85786-104-24 | 8578601042485786010424 | 24 TABLET, FILM COATED in 1 BOTTLE (85786-104-24)Marketed from Aug 18, 2025 |
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)
- Dr Simi All Day Pain Relief
- Generic name (nonproprietary)
- naproxen sodium
- Active ingredients
- Naproxen sodium — 220 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Farmacias De Similares TX LLCNDC labeler code 85786
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 091353
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 85786-104_3c6d4bb5-eb70-944b-e063-6294a90ae8deSPL ID 3c6d4bb5-eb70-944b-e063-6294a90ae8deSPL set ID 3c6d4bb5-eb6f-944b-e063-6294a90ae8deRxCUI 849574UNII 9TN87S3A3CUPC 0850072692876
- 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
N485786010424followed by a unit qualifier and the quantityPackage 85786-0104-24. 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)
Directions Do not take more than directed. The smallest effective dose should be used Drink a full glass of water with each dose. Adults and children 12 years and over: Take 1 caplet every 8 to 12 hours while symptoms last. For the first dose you may take 2 caplets within the first hour. Do not exceed 2 caplets in any 8-12 hour period. Do not exceed 3 caplets in a 24-hour period. Children under 12 years: Ask a doctor.
Excerpt only. Read the full label for complete information.
About NDC 85786-104
- What is NDC 85786-104?
- 85786-104 is the product NDC for Dr Simi All Day Pain Relief (naproxen sodium), Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by Farmacias De Similares TX LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Dr Simi All Day Pain Relief (Naproxen sodium).
- What is the active ingredient?
- Naproxen sodium.
- Who is the labeler?
- Farmacias De Similares TX LLC, NDC labeler code 85786. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Dr Simi All Day 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 091353
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 tablets, 220 mg | Naproxen sodium 220 mg/1 | TabletOral | HealthLife of USA LLC | 69517-109 |
| Naproxen | Naproxen sodium 220 mg/1 | TabletOral | Safeway, Inc | 21130-062 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | TARGET CORPORATION | 11673-764 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Safeway, Inc | 21130-061 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | CVS | 51316-761 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | CVS | 51316-762 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules India Ltd | 62207-327 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules India Ltd | 62207-328 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules India Ltd | 62207-728 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules India Ltd | 62207-729 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Granules India Ltd | 62207-761 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Granules India Ltd | 62207-762 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coated, Extended releaseOral | SPIRIT PHARMACEUTICALS,LLC | 68210-4096 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules USA, Inc. | 69848-010 |
| Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Gobrands, Inc | 82501-1576 |
| Proxen Np 660naproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | OPMX LLC | 69729-123 |
| Rapidol Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Pharmadel LLC | 55758-048 |