arthritis pain relief
- Product NDC
- 41250-658
- 11-digit product format
- 412500658
- Labeler code
- 41250
- Product ID
- 41250-658_24353a73-4f9e-68ba-e063-6394a90ac0b2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Meijer
- Application
- ANDA211544
- Marketing category
- ANDA
- Marketing start
- 2020-03-06
- Marketing end
- 2026-11-30
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- arthritis pain relief
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 650 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 1148399 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41250-658-03 | arthritis pain relief | 1 in 1 CARTON | TABLET, EXTENDED RELEASE | 1 | | 3 |
| 41250-658-03 | arthritis pain relief | 100 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41250-658 | ARTHRITIS PAIN RELIEF (ACETAMINOPHEN) TABLET, EXTENDED RELEASE [MEIJER] | 3 | Current NDC, Legacy NDC, 2 package rows | 20241013_9f03fdb0-7dc0-376e-e053-2995a90ace05.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-658-03 | 41250065803 | 1 BOTTLE, PLASTIC in 1 CARTON (41250-658-03) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC | 2020-03-06 | 2026-11-30 | No | No | Current |