8HR Arthritis Pain Relief
- Product NDC
- 51316-969
- 11-digit product format
- 513160969
- Labeler code
- 51316
- Product ID
- 51316-969_50839010-7c69-159b-e063-6394a90aadfa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen 650mg
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA215486
- Marketing category
- ANDA
- Marketing start
- 2025-07-01
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- 8HR Arthritis Pain Relief
- Listing expiration
- 2027-12-31
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 |
|---|
| 51316-969-01 | 8HR Arthritis Pain Relief | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 51316-969-01 | 51316096901 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (51316-969-01) | 2025-07-01 | No | No | Current |