Acetaminophen
- Product NDC
- 60687-924
- 11-digit product format
- 606870924
- Labeler code
- 60687
- Product ID
- 60687-924_4a0449b1-7dd9-f323-e063-6294a90ac587
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA207229
- Marketing category
- ANDA
- Marketing start
- 2026-02-01
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Acetaminophen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 650 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 1148399 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-924-11 | Acetaminophen | 1 in 1 BLISTER PACK | TABLET | 1 | | 1 |
| 60687-924-21 | Acetaminophen | 30 in 1 CARTON | TABLET | 30 | | 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 |
|---|
| 60687-924-11 | 60687092411 | 1 in 1 BLISTER PACK | | | | | Historical |
| 60687-924-21 | 60687092421 | 30 BLISTER PACK in 1 CARTON (60687-924-21) / 1 TABLET in 1 BLISTER PACK (60687-924-11) | 30 blister pack | 2026-02-01 | No | No | Historical |