Acetaminophen
- Product NDC
- 42912-0152
- 11-digit product format
- 429120152
- Labeler code
- 42912
- Product ID
- 42912-0152_896e0b77-09de-4832-9c3d-d273005e5b43
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TDS Pharm Co., Ltd
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-07-15
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42912-0152-7 | Acetaminophen | 1 in 1 BOX | TABLET | 1 | | 1 |
| 42912-0152-7 | Acetaminophen | 40 in 1 BOTTLE | TABLET | 40 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42912-0152 | ACETAMINOPHEN TABLET [TDS PHARM CO., LTD] | 1 | Legacy NDC, 2 package rows | 20100820_c3b408ff-f47b-4fee-ade5-5db6e25f4ee0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 42912-0152-7 | 42912015207 | 1 in 1 BOX | Historical |