Pharbetol
- Product NDC
- 73057-376
- 11-digit product format
- 730570376
- Labeler code
- 73057
- Product ID
- 73057-376_2b899f07-4c46-cd87-e063-6294a90a4090
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen 500mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Ulai Health LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-07-08
- Substance
- ACETAMINOPHEN
- Active strength
- 500 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
- Pharbetol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 198440, 1293942 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73057-376-08 | Pharbetol | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 3 |
| 73057-376-11 | Pharbetol | 1000 in 1 BOTTLE, PLASTIC | TABLET | 1000 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73057-376 | PHARBETOL (ACETAMINOPHEN 500MG) TABLET [ULAI HEALTH LLC] | 3 | Current NDC, Legacy NDC, 2 package rows | 20250114_e64ce7b1-4501-4b51-b012-1882ed153b42.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 |
|---|
| 73057-376-08 | 73057037608 | 100 TABLET in 1 BOTTLE, PLASTIC (73057-376-08) | 100 tablet | 2019-07-08 | 0000-00-00 | No | No | Current |
| 73057-376-11 | 73057037611 | 1000 TABLET in 1 BOTTLE, PLASTIC (73057-376-11) | 1000 tablet | 2019-07-08 | 0000-00-00 | No | No | Current |