All Night Pain Relief PM
- Product NDC
- 0363-0844
- 11-digit product format
- 003630844
- Labeler code
- 0363
- Product ID
- 0363-0844_022bd9fe-6d43-4ca8-8dd8-4ecb2c198a85
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Walgreens
- Application
- ANDA209726
- Marketing category
- ANDA
- Marketing start
- 2018-12-31
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0844 | ALL NIGHT PAIN RELIEF PM (NAPROXEN SODIUM) TABLET [WALGREENS] | 4 | Legacy NDC | 20250509_12ab219a-051c-4e54-98e1-32cb3689586e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-0844-80 | 00363084480 | 80 TABLET in 1 BOTTLE, PLASTIC (0363-0844-80) | 80 tablet | 2018-12-31 | 0000-00-00 | No | No | Current |