Pharbetol
- Product NDC
- 67046-023
- 11-digit product format
- 670460023
- Labeler code
- 67046
- Product ID
- 67046-023_bc1cdbdb-b3ec-2397-e053-2995a90a9c81
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Coupler Enterprises
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2007-01-09
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 325 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 67046-023-30 | PharbetolRegular strength | 30 in 1 BLISTER PACK | TABLET | 30 | | 3 |
| 67046-023-60 | PharbetolRegular strength | 60 in 1 BLISTER PACK | TABLET | 60 | | 3 |
| 67046-023-62 | PharbetolRegular strength | 60 in 1 BLISTER PACK | TABLET | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-023 | PHARBETOL REGULAR STRENGTH (ACETAMINOPHEN) TABLET [COUPLER ENTERPRISES] | 3 | Legacy NDC, 3 package rows | 20210225_57e5fc8c-8d69-a36d-e053-2a91aa0af949.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 |
|---|
| 67046-023-30 | 67046002330 | 30 TABLET in 1 BLISTER PACK (67046-023-30) | 30 tablet | 2007-01-09 | 0000-00-00 | No | No | Current |
| 67046-023-60 | 67046002360 | 60 TABLET in 1 BLISTER PACK (67046-023-60) | 60 tablet | 2007-01-09 | 0000-00-00 | No | No | Current |
| 67046-023-62 | 67046002362 | 60 TABLET in 1 BLISTER PACK (67046-023-62) | 60 tablet | 2007-01-09 | 0000-00-00 | No | No | Current |