Arthritis Pain Reliever
- Product NDC
- 55700-679
- 11-digit product format
- 557000679
- Labeler code
- 55700
- Product ID
- 55700-679_ba9973d2-beb9-485a-9aaf-5f02ee9b130b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA076200
- Marketing category
- ANDA
- Marketing start
- 2018-09-07
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-679-30 | 55700067930 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55700-679-30) | 2018-09-07 | 0000-00-00 | No | No | Current |