Arthritis Pain Reliever
- Product NDC
- 68071-1552
- 11-digit product format
- 680711552
- Labeler code
- 68071
- Product ID
- 68071-1552_d6ac3eab-1724-33f5-e053-2995a90a748c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076200
- Marketing category
- ANDA
- Marketing start
- 2002-04-30
- 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
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 |
|---|
| 68071-1552-5 | 68071155205 | 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-1552-5) | 2017-09-29 | 0000-00-00 | No | No | Current |