Arthritis Pain Reliever
- Product NDC
- 30142-970
- 11-digit product format
- 301420970
- Labeler code
- 30142
- Product ID
- 30142-970_be2cae5f-8d4d-4be7-9d6b-588444e2f804
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- The Kroger Company
- Application
- ANDA076200
- Marketing category
- ANDA
- Marketing start
- 2021-02-19
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 30142-970 | ARTHRITIS PAIN RELIEVER (ACETAMINOPHEN) TABLET, FILM COATED, EXTENDED RELEASE [THE KROGER COMPANY] | 3 | Legacy NDC | 20250114_d81ee7dc-abe0-4d41-9176-6311b80dace3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30142-970-01 | 30142097001 | 1 BOTTLE in 1 CARTON (30142-970-01) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2021-02-19 | 0000-00-00 | No | No | Current |