LEADER Ultra Strength
- Product NDC
- 70000-0459
- 11-digit product format
- 700000459
- Labeler code
- 70000
- Product ID
- 70000-0459_1ef40df3-78e7-4323-bfd2-e16abecce29c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chewable Antacid Tablets
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-12-18
- Substance
- CALCIUM CARBONATE
- Active strength
- 1000 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LEADER Ultra Strength
- Brand name suffix
- Peppermint Flavor
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM CARBONATE | 1000 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H0G9379FGK |
| Rxcui | 308892 |
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 |
|---|
| 70000-0459-1 | LEADER Ultra StrengthPeppermint Flavor | 72 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 72 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70000-0459 | LEADER ULTRA STRENGTH PEPPERMINT FLAVOR (CHEWABLE ANTACID TABLETS) TABLET, CHEWABLE [CARDINAL HEALTH] | 12 | Current NDC, Legacy NDC, 1 package rows | 20241122_3bf16b23-5a67-454f-b335-677cc49cd7a3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70000-0459-1 | 70000045901 | 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (70000-0459-1) | 2018-12-18 | 0000-00-00 | No | No | Current |