Naproxen Sodium
- Product NDC
- 30142-748
- 11-digit product format
- 301420748
- Labeler code
- 30142
- Product ID
- 30142-748_e02ba5d6-1d30-4bea-abd8-1327807e280c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- The Kroger Co.
- Application
- ANDA208363
- Marketing category
- ANDA
- Marketing start
- 2018-04-01
- Marketing end
- 2024-05-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30142-748-12 | 30142074812 | 1 BOTTLE, PLASTIC in 1 BOX (30142-748-12) > 120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | | 2018-04-01 | 0000-00-00 | No | No | Current |
| 30142-748-16 | 30142074816 | 1 BOTTLE in 1 BOX (30142-748-16) > 160 CAPSULE, LIQUID FILLED in 1 BOTTLE | 1 bottle | 2018-04-01 | 0000-00-00 | No | No | Current |
| 30142-748-80 | 30142074880 | 80 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-748-80) | | 2018-04-01 | 0000-00-00 | No | No | Current |