Over-the-counter drug · ANDA
basic care naproxen sodium pm NDC 72288-310
diphenhydramine hydrochloride, naproxen sodium · Diphenhydramine hydrochloride 25 mg/1; 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 |
|---|---|---|---|
| 72288-310-06 | 7228803100672288031006 | 1 BOTTLE in 1 CARTON (72288-310-06) / 160 TABLET, FILM COATED in 1 BOTTLEMarketed from Aug 10, 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)
- basic care naproxen sodium pm
- Generic name (nonproprietary)
- diphenhydramine hydrochloride, naproxen sodium
- Active ingredients
- Diphenhydramine hydrochloride — 25 mg/1Naproxen sodium — 220 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Amazon.com Services LLCNDC labeler code 72288
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 208499
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Histamine H1 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 72288-310_c9655163-d65d-457c-843d-247fc595d36bSPL ID c9655163-d65d-457c-843d-247fc595d36bSPL set ID 7beed9e7-816b-494b-93fa-9caf10aa3834RxCUI 1550957UNII TC2D6JAD40, 9TN87S3A3C
- Pharmacologic class
- Histamine-1 Receptor Antagonist; 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
N472288031006followed by a unit qualifier and the quantityPackage 72288-0310-06. 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 • for relief of occasional sleeplessness when associated with minor aches and pains • helps you fall asleep and stay asleep
Excerpt only. Read the full label for complete information.
About NDC 72288-310
- What is NDC 72288-310?
- 72288-310 is the product NDC for basic care naproxen sodium pm, Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by Amazon.com Services LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- basic care naproxen sodium pm (Diphenhydramine hydrochloride, naproxen sodium).
- What is the active ingredient?
- Diphenhydramine hydrochloride, Naproxen sodium.
- Who is the labeler?
- Amazon.com Services LLC, NDC labeler code 72288. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for basic care naproxen sodium pm?
- 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 208499
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 Night Pain Relief PMdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Walgreen Company | 0363-2264 |
| careone naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | American Sales Company | 41520-264 |
| dg health naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Dolgencorp Inc | 55910-858 |
| equaline naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | United Natural Foods, Inc. dba UNFI | 41163-593 |
| good sense naproxen sodiumdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | L. Perrigo Company | 0113-8264 |
| Naproxen Sodium PMdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Safeway | 21130-639 |
| naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | TabletOral | Kroger Company | 30142-753 |
| naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | H E B | 37808-264 |
| naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Meijer Distribution Inc | 41250-526 |
| topcare all night pain relief pmdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Topco Associates LLC | 36800-264 |
| up and up naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Target Corporation | 11673-687 |