Acetaminophen Extra Strength
- Product NDC
- 37835-507
- 11-digit product format
- 378350507
- Labeler code
- 37835
- Product ID
- 37835-507_371d5ff5-bfe9-1a6f-e063-6294a90a3b19
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bi-Mart
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-05-01
- 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 |
|---|
| 37835-507-01 | Acetaminophen Extra Strength | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 37835-507-05 | Acetaminophen Extra Strength | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
| 37835-507-25 | Acetaminophen Extra Strength | 250 in 1 BOTTLE | TABLET | 250 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 37835-507-01 | 37835050701 | 100 TABLET in 1 BOTTLE (37835-507-01) | 100 tablet | 2025-05-01 | No | No | Historical |
| 37835-507-05 | 37835050705 | 500 TABLET in 1 BOTTLE (37835-507-05) | 500 tablet | 2025-05-01 | No | No | Historical |
| 37835-507-25 | 37835050725 | 250 TABLET in 1 BOTTLE (37835-507-25) | 250 tablet | 2025-05-01 | No | No | Historical |