ArthritisPain Relief
- Product NDC
- 59726-669
- 11-digit product format
- 597260669
- Labeler code
- 59726
- Product ID
- 59726-669_562b15d7-4b70-44cc-acde-54f0269728bc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA207035
- Marketing category
- ANDA
- Marketing start
- 2021-04-30
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59726-669 | ARTHRITISPAIN RELIEF (ACETAMINOPHEN) TABLET [P & L DEVELOPMENT, LLC] | 3 | Legacy NDC | 20241103_4d27405b-a384-43a0-af15-43378d30b9f4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-669-10 | 59726066910 | 1 BOTTLE, PLASTIC in 1 BOX (59726-669-10) > 100 TABLET in 1 BOTTLE, PLASTIC | 2021-04-30 | 0000-00-00 | No | No | Current |