ACETAMINOPHEN
- Product NDC
- 68210-0022
- 11-digit product format
- 682100022
- Labeler code
- 68210
- Product ID
- 68210-0022_eeca6dcf-c8c4-7cf9-e053-2995a90a936a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- SPIRIT PHARMACEUTICALS LLC
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-05-19
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 325 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68210-0022-1 | ACETAMINOPHEN | 100 in 1 BOTTLE | TABLET | 100 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68210-0022 | ACETAMINOPHEN TABLET [SPIRIT PHARMACEUTICALS LLC] | 8 | Legacy NDC, 1 package rows | 20241211_e36a4e7b-c4a3-498c-81bd-ca8e1a3e120b.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 |
|---|
| 68210-0022-1 | 68210002201 | 100 TABLET in 1 BOTTLE (68210-0022-1) | 100 tablet | 2017-05-19 | 0000-00-00 | No | No | Current |