Acetaminophen Caplets
- Product NDC
- 70729-001
- 11-digit product format
- 707290001
- Labeler code
- 70729
- Product ID
- 70729-001_62ddc12d-7480-4db8-a784-e2e1503fad2b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Breeden Brothers, LLC
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-05-01
- 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
- Acetaminophen Caplets
- 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 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70729-001-24 | Acetaminophen Caplets | 24 in 1 BOTTLE, PLASTIC | TABLET | 24 | | 2 |
| 70729-001-50 | Acetaminophen Caplets | 50 in 1 BOTTLE, PLASTIC | TABLET | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70729-001 | ACETAMINOPHEN CAPLETS (ACETAMINOPHEN) TABLET [BREEDEN BROTHERS, LLC] | 2 | Current NDC, Legacy NDC, 2 package rows | 20180929_57fff3dc-ba30-4d3d-9362-01df6974f813.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 |
|---|
| 70729-001-24 | 70729000124 | 24 TABLET in 1 BOTTLE, PLASTIC (70729-001-24) | 24 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |
| 70729-001-50 | 70729000150 | 50 TABLET in 1 BOTTLE, PLASTIC (70729-001-50) | 50 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |