ALL DAY PAIN RELIEF
- Product NDC
- 68210-0030
- 11-digit product format
- 682100030
- Labeler code
- 68210
- Product ID
- 68210-0030_9aa38918-34a3-1b8f-e053-2a95a90ad14d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- NAPROXEN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- SPIRIT PHARMACEUTICALS LLC
- Application
- ANDA090545
- Marketing category
- ANDA
- Marketing start
- 2018-04-11
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68210-0030-1 | ALL DAY PAIN RELIEF | 15 in 1 BOTTLE | TABLET | 15 | | 2 |
| 68210-0030-1 | ALL DAY PAIN RELIEF | 1 in 1 CARTON | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68210-0030 | ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [SPIRIT PHARMACEUTICALS LLC] | 2 | Legacy NDC, 2 package rows | 20191227_2a8df549-613b-4fdb-8251-e6d63078e103.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68210-0030-1 | 68210003001 | 1 BOTTLE in 1 CARTON (68210-0030-1) > 15 TABLET in 1 BOTTLE | 1 bottle | 2018-04-11 | 0000-00-00 | No | No | Current |