Acetaminophen
- Product NDC
- 17714-012
- 11-digit product format
- 177140012
- Labeler code
- 17714
- Product ID
- 17714-012_60f41580-e068-faad-e053-2a91aa0a9076
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advance Pharmaceutical Inc.
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 1989-02-05
- Substance
- ACETAMINOPHEN
- Active strength
- 325 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
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 325 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 313782 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17714-012-01 | Acetaminophen | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 17714-012-10 | Acetaminophen | 1000 in 1 BOTTLE | TABLET | 1000 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17714-012 | ACETAMINOPHEN TABLET [ADVANCE PHARMACEUTICAL INC.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20171223_3793a17e-13bf-4d27-b8fa-6753b760f820.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 |
|---|
| 17714-012-01 | 17714001201 | 100 TABLET in 1 BOTTLE (17714-012-01) | 100 tablet | 1989-02-05 | 0000-00-00 | No | No | Current |
| 17714-012-10 | 17714001210 | 1000 TABLET in 1 BOTTLE (17714-012-10) | 1000 tablet | 1989-02-05 | 0000-00-00 | No | No | Current |