ACETAMINOPHEN 500 MG
- Product NDC
- 72090-038
- 11-digit product format
- 720900038
- Labeler code
- 72090
- Product ID
- 72090-038_2d0de82a-1213-40ed-9e49-d6d1c36c015e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Pioneer Life Sciences, LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-01-09
- 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 500 MG
- 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 |
|---|
| 72090-038-01 | ACETAMINOPHEN 500 MG | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
| 72090-038-02 | ACETAMINOPHEN 500 MG | 300 in 1 PACKAGE | TABLET | 300 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72090-038 | ACETAMINOPHEN 500 MG (ACETAMINOPHEN) TABLET [PIONEER LIFE SCIENCES, LLC] | 1 | Current NDC, 2 package rows | 20250110_e817bc4a-43ef-4126-b903-aabd1390cd0c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72090-038-01 | 72090003801 | 500 TABLET in 1 BOTTLE (72090-038-01) | 500 tablet | 2025-01-09 | No | No | Current |
| 72090-038-02 | 72090003802 | 300 TABLET in 1 PACKAGE (72090-038-02) | 300 tablet | 2025-01-09 | No | No | Current |