8 Hour Pain Relief
- Product NDC
- 63868-679
- 11-digit product format
- 638680679
- Labeler code
- 63868
- Product ID
- 63868-679_24357a94-9aa7-4606-e063-6294a90ad492
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- CHAIN DRUG MARKETING ASSOCIATION INC
- Application
- ANDA211544
- Marketing category
- ANDA
- Marketing start
- 2020-08-01
- Marketing end
- 2027-01-31
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- 8 Hour 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63868-679-50 | 8 Hour Pain Relief | 1 in 1 CARTON | TABLET, EXTENDED RELEASE | 1 | | 3 |
| 63868-679-50 | 8 Hour Pain Relief | 50 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 50 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63868-679 | 8 HOUR PAIN RELIEF (ACETAMINOPHEN) TABLET, EXTENDED RELEASE [CHAIN DRUG MARKETING ASSOCIATION INC] | 3 | Current NDC, Legacy NDC, 2 package rows | 20241013_1da0bd23-9f26-4913-9ebf-1fd8b0fb3bd3.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 |
|---|
| 63868-679-50 | 63868067950 | 1 BOTTLE, PLASTIC in 1 CARTON (63868-679-50) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC | 2020-08-01 | 2027-01-31 | No | No | Current |