Arthritis Pain Reliever
- Product NDC
- 50268-052
- 11-digit product format
- 502680052
- Labeler code
- 50268
- Product ID
- 50268-052_d5cbb27d-91f9-1acd-e053-2a95a90acd87
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA076200
- Marketing category
- ANDA
- Marketing start
- 2016-03-07
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50268-052 | ARTHRITIS PAIN RELIEVER (ACETAMINOPHEN) TABLET, FILM COATED, EXTENDED RELEASE [AVPAK] | 6 | Legacy NDC | 20240110_fa9c5660-2e9a-3f2c-ae1e-f77af543e877.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-052-15 | 50268005215 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-052-15) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (50268-052-11) | 50 blister pack | 2016-03-07 | 0000-00-00 | No | No | Current |