PANADOL
- Product NDC
- 0135-0539
- 11-digit product format
- 001350539
- Labeler code
- 0135
- Product ID
- 0135-0539_10c14ee5-017b-0434-e063-6394a90af0f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Haleon US Holdings LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-10-15
- Substance
- ACETAMINOPHEN
- Active strength
- 160 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PANADOL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 160 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0135-0539-02 | PANADOL | 1 in 1 CARTON | SUSPENSION | 1 | | 10 |
| 0135-0539-02 | PANADOL | 54.7 mL in 1 BOTTLE | SUSPENSION | 54.7 | | 10 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0135-0539 | PANADOL (ACETAMINOPHEN) SUSPENSION [HALEON US HOLDINGS LLC] | 10 | Current NDC, Legacy NDC, 2 package rows | 20240207_95801755-db54-4ad7-bec1-52671914f6ca.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0135-0539-02 | 00135053902 | 1 BOTTLE in 1 CARTON (0135-0539-02) / 54.7 mL in 1 BOTTLE | 1 bottle | 2012-10-15 | 0000-00-00 | No | No | Current |