ANTACID
- Product NDC
- 70000-0683
- 11-digit product format
- 700000683
- Labeler code
- 70000
- Product ID
- 70000-0683_411d7abc-9cd4-0480-e063-6394a90a8bb8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- calcium carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- CARDINAL HEALTH 110, LLC.
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-07-08
- Substance
- CALCIUM CARBONATE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ANTACID
- Brand name suffix
- Ultra Strength
- Listing expiration
- 2026-12-31
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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70000-0683-1 | ANTACIDUltra Strength | 72 in 1 BOTTLE | TABLET, CHEWABLE | 72 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70000-0683 | ANTACID ULTRA STRENGTH (CALCIUM CARBONATE) TABLET, CHEWABLE [CARDINAL HEALTH 110, LLC.] | 2 | Current NDC, 1 package rows | 20241128_d267ca31-09bd-46d3-be08-a259642f1b7f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70000-0683-1 | 70000068301 | 72 TABLET, CHEWABLE in 1 BOTTLE (70000-0683-1) | 2024-07-08 | No | No | Historical |