Leader All Day Pain Relief
- Product NDC
- 70000-0201
- 11-digit product format
- 700000201
- Labeler code
- 70000
- Product ID
- 70000-0201_d57f5c20-608d-4543-baa7-07566acd7b68
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health 110, LLC. dba Leader
- Application
- ANDA074661
- Marketing category
- ANDA
- Marketing start
- 2016-12-07
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Leader All Day Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NAPROXEN SODIUM | 220 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9TN87S3A3C |
| Rxcui | 849574 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70000-0201-1 | Leader All Day Pain Relief | 200 in 1 BOTTLE | TABLET, FILM COATED | 200 | | 11 |
| 70000-0201-1 | Leader All Day Pain Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 11 |
| 70000-0201-2 | Leader All Day Pain Relief | 50 in 1 BOTTLE | TABLET, FILM COATED | 50 | | 11 |
| 70000-0201-2 | Leader All Day Pain Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 11 |
| 70000-0201-3 | Leader All Day Pain Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 11 |
| 70000-0201-3 | Leader All Day Pain Relief | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 11 |
| 70000-0201-4 | Leader All Day Pain Relief | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | | 11 |
| 70000-0201-4 | Leader All Day Pain Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 11 |
| 70000-0201-5 | Leader All Day Pain Relief | 24 in 1 BOTTLE | TABLET, FILM COATED | 24 | | 11 |
| 70000-0201-5 | Leader All Day Pain Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 11 |
| 70000-0201-6 | Leader All Day Pain Relief | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 11 |
| 70000-0201-6 | Leader All Day Pain Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70000-0201 | LEADER ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [CARDINAL HEALTH 110, LLC. DBA LEADER] | 10 | Current NDC, Legacy NDC, 12 package rows | 20230617_b01c2b4e-a092-42dc-a387-d181d8ba14bb.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 |
|---|
| 70000-0201-1 | 70000020101 | 1 BOTTLE in 1 CARTON (70000-0201-1) > 200 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2016-12-07 | 2022-01-31 | No | No | Current |
| 70000-0201-2 | 70000020102 | 1 BOTTLE in 1 CARTON (70000-0201-2) / 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-02-16 | 0000-00-00 | No | No | Current |
| 70000-0201-3 | 70000020103 | 1 BOTTLE in 1 CARTON (70000-0201-3) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-02-16 | 0000-00-00 | No | No | Current |
| 70000-0201-4 | 70000020104 | 1 BOTTLE in 1 CARTON (70000-0201-4) > 120 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-06-27 | 0000-00-00 | No | No | Current |
| 70000-0201-5 | 70000020105 | 1 BOTTLE in 1 CARTON (70000-0201-5) / 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2021-09-21 | 0000-00-00 | No | No | Current |
| 70000-0201-6 | 70000020106 | 1 BOTTLE in 1 CARTON (70000-0201-6) / 90 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2022-06-07 | 0000-00-00 | No | No | Current |