Arthritis Pain
- Product NDC
- 21130-124
- 11-digit product format
- 211300124
- Labeler code
- 21130
- Product ID
- 21130-124_af0b0908-30f5-2cce-e053-2995a90a007d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- SAFEWAY
- Application
- ANDA211544
- Marketing category
- ANDA
- Marketing start
- 2020-01-01
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-124 | ARTHRITIS PAIN (ACETAMINOPHEN) TABLET, EXTENDED RELEASE [SAFEWAY] | 5 | Legacy NDC | 20231031_968a3a90-622b-b17f-e053-2995a90aed66.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21130-124-02 | 21130012402 | 1 BOTTLE, PLASTIC in 1 CARTON (21130-124-02) > 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC | 2020-01-01 | 0000-00-00 | No | No | Current |
| 21130-124-03 | 21130012403 | 1 BOTTLE, PLASTIC in 1 CARTON (21130-124-03) > 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC | 2020-01-01 | 0000-00-00 | No | No | Current |