arthritis pain
- Product NDC
- 30142-789
- 11-digit product format
- 301420789
- Labeler code
- 30142
- Product ID
- 30142-789_fa1a1cdc-6d40-48b3-8541-5d1be2b6aaa2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA075077
- Marketing category
- ANDA
- Marketing start
- 2019-10-03
- Marketing end
- 2023-08-31
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30142-789-83 | 30142078983 | 225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (30142-789-83) | 2019-10-03 | 0000-00-00 | No | No | Current |