Over-the-counter drug · ANDA
All Night Pain Relief PM NDC 0363-2264
diphenhydramine hydrochloride, naproxen sodium · Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 · Tablet, Film coated · Oral · Walgreen Company
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0363-2264-27 | 00363226427 | 1 BOTTLE in 1 CARTON (0363-2264-27) / 80 TABLET, FILM COATED in 1 BOTTLE (0363-2264-80)Marketed from Apr 27, 2026 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 Night Pain Relief 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
- Walgreen Company
- 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 0363-2264_81c4f94d-6f5e-4e69-940b-b94b3533963cSPL ID 81c4f94d-6f5e-4e69-940b-b94b3533963cSPL set ID 43e4ed28-b1be-4548-86ac-f40f9f83f04eRxCUI 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
N400363226427followed by a unit qualifier and the quantityPackage 00363-2264-27. 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.
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 |
|---|---|---|---|---|
| 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 | Safeway | 21130-639 |
| basic care naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-310 |
| 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 |
| 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 |
| 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 |
| naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Meijer Distribution Inc | 41250-526 |
| 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 |
| 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 |
| 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 |
| naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium | Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | H E B | 37808-264 |