Harris Teeter Arthritis Pain
- Product NDC
- 69256-966
- 11-digit product format
- 692560966
- Labeler code
- 69256
- Product ID
- 69256-966_3809e367-3e36-473a-8187-999f3e006c80
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Harris Teeter, LLC
- Application
- ANDA075077
- Marketing category
- ANDA
- Marketing start
- 2015-11-21
- 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 |
|---|
| 69256-966 | HARRIS TEETER ARTHRITIS PAIN (ACETAMINOPHEN) TABLET, FILM COATED, EXTENDED RELEASE [HARRIS TEETER, LLC] | 3 | Legacy NDC | 20200225_bcc6d794-330f-4aff-9cbe-e4e8f29c2e22.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69256-966-83 | 69256096683 | 225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69256-966-83) | 2015-11-21 | 0000-00-00 | No | No | Current |