Members Mark Arthritis Pain
- Product NDC
- 68196-611
- 11-digit product format
- 681960611
- Labeler code
- 68196
- Product ID
- 68196-611_77d60018-88b8-4d09-8226-27c66ddce3da
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Sam's West Inc
- Application
- ANDA075077
- Marketing category
- ANDA
- Marketing start
- 2025-11-20
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Members Mark Arthritis Pain
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 650 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 1148399 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68196-611-82 | Members Mark Arthritis Pain | 200 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 200 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68196-611-82 | 68196061182 | 200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68196-611-82) | 2025-11-20 | No | No | Current |