Uline Acetaminophen Extra Strength
- Product NDC
- 69790-154
- 11-digit product format
- 697900154
- Labeler code
- 69790
- Product ID
- 69790-154_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
- 2024-01-30
- 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 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 69790-154-33 | 69790015433 | 50 PACKET in 1 BOX (69790-154-33) / 2 TABLET, FILM COATED in 1 PACKET | 50 packet | 2024-01-30 | No | No | Historical |