EC-NAPROXEN
- Product NDC
- 69784-500
- 11-digit product format
- 697840500
- Labeler code
- 69784
- Product ID
- 69784-500_e7975860-648a-454a-b324-9d7824f92521
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- naproxen
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Woodward Pharma Services LLC
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69784-500 | NAPROXEN TABLET EC-NAPROXEN (NAPROXEN) TABLET, DELAYED RELEASE NAPROXEN SODIUM DS (NAPROXEN SODIUM) TABLET [WOODWARD PHARMA SERVICES LLC] | 5 | Legacy NDC | 20240415_0728935b-19fc-4a10-aeba-29c42ce7f472.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69784-500-01 | 69784050001 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69784-500-01) | 2018-10-15 | 0000-00-00 | No | No | Current |