Acetaminophen
- Product NDC
- 63739-440
- 11-digit product format
- 637390440
- Labeler code
- 63739
- Product ID
- 63739-440_c741047f-2c14-1220-e053-2a95a90aecb4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Packaging Services Business Unit of McKesson Corporation
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2009-03-01
- Marketing end
- 2021-07-31
- Substance
- ACETAMINOPHEN
- Active strength
- 325 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
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 |
|---|
| 63739-440-01 | 63739044001 | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-440-01) > 30 TABLET in 1 BLISTER PACK | 25 blister pack | 2009-04-30 | 2021-07-31 | No | No | Current |