Uline Acetaminophen Extra Strength
- Product NDC
- 69790-804
- 11-digit product format
- 697900804
- Labeler code
- 69790
- Product ID
- 69790-804_3e5d8ade-be5f-4cfa-e063-6394a90a99f6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Uline
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-10-07
- 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
- Uline Acetaminophen Extra Strength
- 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 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69790-804-33 | Uline Acetaminophen Extra Strength | 50 in 1 BOX | TABLET, FILM COATED | 50 | | 8 |
| 69790-804-33 | Uline Acetaminophen Extra Strength | 2 in 1 PACKET | TABLET, FILM COATED | 2 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69790-804 | ULINE ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [ULINE] | 7 | Current NDC, Legacy NDC, 2 package rows | 20240131_90167594-0a49-2492-e053-2a95a90a1401.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 |
|---|
| 69790-804-33 | 69790080433 | 50 PACKET in 1 BOX (69790-804-33) / 2 TABLET, FILM COATED in 1 PACKET | 50 packet | 2019-10-07 | 0000-00-00 | No | No | Current |