Acetaminophen
- Product NDC
- 69848-003
- 11-digit product format
- 698480003
- Labeler code
- 69848
- Product ID
- 69848-003_468e5f4e-8bc6-6b97-e063-6294a90a0166
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Granules USA, Inc
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-07-01
- Substance
- ACETAMINOPHEN
- Active strength
- 500 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
- Acetaminophen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 198440 |
FDA-Initiated Inactive NDC Indexing#
NDC, Effective, Action table| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|
| 69848-003-10 | 2020-12-30 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
| 69848-003-17 | 2020-12-30 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
| 69848-003-24 | 2020-12-30 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
| 69848-003-10 | 2020-09-27 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
| 69848-003-17 | 2020-09-27 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
| 69848-003-24 | 2020-09-27 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
| 69848-003-10 | 2020-09-25 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
| 69848-003-17 | 2020-09-25 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
| 69848-003-24 | 2020-09-25 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
| 69848-003-10 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
| 69848-003-17 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
| 69848-003-24 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-277a-f274-e053-dbdaa90a6471 | EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69848-003-10 | Acetaminophen | 100 in 1 BOTTLE | TABLET | 100 | | 8 |
| 69848-003-17 | Acetaminophen | 175 in 1 BOTTLE | TABLET | 175 | | 8 |
| 69848-003-24 | Acetaminophen | 24 in 1 BOTTLE | TABLET | 24 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69848-003 | ACETAMINOPHEN TABLET [GRANULES USA, INC] | 7 | Current NDC, Legacy NDC, 3 package rows | 20241218_a1255f60-b9c6-9a95-e053-2995a90a9e80.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69848-003-10 | 69848000310 | 100 TABLET in 1 BOTTLE (69848-003-10) | 100 tablet | 2019-07-01 | 0000-00-00 | No | No | Current |
| 69848-003-17 | 69848000317 | 175 TABLET in 1 BOTTLE (69848-003-17) | 175 tablet | 2019-07-01 | 0000-00-00 | No | No | Current |
| 69848-003-24 | 69848000324 | 24 TABLET in 1 BOTTLE (69848-003-24) | 24 tablet | 2019-07-01 | 0000-00-00 | No | No | Current |