All Day Pain Relief
- Product NDC
- 33992-0169
- 11-digit product format
- 339920169
- Labeler code
- 33992
- Product ID
- 33992-0169_4f1b212f-7eaa-463b-b9a3-53c327b616fd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ASSURED / DOLLAR TREE (Greenbrier International, Inc.)
- Application
- ANDA079096
- Marketing category
- ANDA
- Marketing start
- 2020-03-13
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], 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 |
|---|
| 33992-0169 | ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [ASSURED / DOLLAR TREE (GREENBRIER INTERNATIONAL, INC.)] | 3 | Legacy NDC | 20220922_b35947f1-efa0-4779-aa18-e04425824fa1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 33992-0169-4 | 33992016904 | 1 BOTTLE, PLASTIC in 1 BOX (33992-0169-4) > 24 TABLET in 1 BOTTLE, PLASTIC | 2020-03-13 | 0000-00-00 | No | No | Current |