Acetaminophen Extra Strength
- Product NDC
- 58602-776
- 11-digit product format
- 586020776
- Labeler code
- 58602
- Product ID
- 58602-776_0b4541a6-ce74-d7e6-e063-6294a90aa709
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aurohealth LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-09-02
- 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 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58602-776-88 | Acetaminophen Extra Strength | 750 in 1 BOTTLE | TABLET | 750 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58602-776 | ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [AUROHEALTH LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231130_57bb1acc-b9a0-48cd-8e5c-33712441ce81.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 |
|---|
| 58602-776-88 | 58602077688 | 750 TABLET in 1 BOTTLE (58602-776-88) | 750 tablet | 2022-09-02 | 0000-00-00 | No | No | Current |