Naproxen Sodium
- Product NDC
- 37808-175
- 11-digit product format
- 378080175
- Labeler code
- 37808
- Product ID
- 37808-175_0f16c5ce-4744-4915-aa19-f6e43d9da0ae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- H E B
- Application
- NDA021920
- Marketing category
- NDA
- Marketing start
- 2015-07-31
- Marketing end
- 2024-01-05
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-175-40 | 37808017540 | 1 BOTTLE, PLASTIC in 1 BOX (37808-175-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2015-07-31 | 2024-01-05 | No | No | Current |
| 37808-175-80 | 37808017580 | 1 BOTTLE, PLASTIC in 1 BOX (37808-175-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2015-07-31 | 2024-01-05 | No | No | Current |