Arthritis Pain Reliever
- Product NDC
- 59726-013
- 11-digit product format
- 597260013
- Labeler code
- 59726
- Product ID
- 59726-013_87fee0eb-ab88-451a-b5d9-2e1d067d4014
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA211544
- Marketing category
- ANDA
- Marketing start
- 2020-04-30
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59726-013 | ARTHRITIS PAIN RELIEVER EXTENDED RELEASE (ACETAMINOPHEN) TABLET [P & L DEVELOPMENT, LLC] | 3 | Legacy NDC | 20241030_0dcf54e7-de0c-426a-9b49-2ac2e8b6bdb0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-013-10 | 59726001310 | 1 BOTTLE, PLASTIC in 1 BOX (59726-013-10) > 100 TABLET in 1 BOTTLE, PLASTIC | 2020-04-30 | 0000-00-00 | No | No | Current |