EC-NAPROXEN
- Product NDC
- 63629-2484
- 11-digit product format
- 636292484
- Labeler code
- 63629
- Product ID
- 63629-2484_e13bdb1a-bed1-4827-87a4-30ee5683bcfa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- naproxen
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA020067
- Marketing category
- NDA
- Marketing start
- 2018-10-15
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN
- Active strength
- 500 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 |
|---|
| 63629-2484 | EC-NAPROXEN (NAPROXEN) TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK] | 104 | Legacy NDC | 20240601_d6443cba-5593-4bd1-8137-af12b4103790.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2484-1 | 63629248401 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63629-2484-1) | 2022-09-07 | 0000-00-00 | No | No | Current |