Arthritis Pain
- Product NDC
- 68196-034
- 11-digit product format
- 681960034
- Labeler code
- 68196
- Product ID
- 68196-034_3c156540-3319-441d-e063-6394a90adced
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- SAM'S WEST INC
- Application
- ANDA215486
- Marketing category
- ANDA
- Marketing start
- 2025-08-20
- 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
- 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 |
|---|
| 68196-034-02 | Arthritis Pain | 200 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 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 |
|---|
| 68196-034-02 | 68196003402 | 200 TABLET, EXTENDED RELEASE in 1 BOTTLE (68196-034-02) | 2025-08-20 | No | No | Current |