Acetaminophen
- Product NDC
- 76168-010
- 11-digit product format
- 761680010
- Labeler code
- 76168
- Product ID
- 76168-010_b3795b58-f7b7-4a62-89c8-23d11e38f44c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Velocity Pharma
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2012-12-05
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76168-010-12 | Acetaminophen | 1 in 1 CARTON | TABLET | 1 | | 1 |
| 76168-010-12 | Acetaminophen | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76168-010 | ACETAMINOPHEN TABLET [VELOCITY PHARMA] | 1 | Legacy NDC, 2 package rows | 20130829_464b1b5b-743b-40bf-8ab5-83c3a4abe9d4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76168-010-12 | 76168001012 | 1 in 1 CARTON | Historical |