Genexa Antacid
- Product NDC
- 69676-0072
- 11-digit product format
- 696760072
- Labeler code
- 69676
- Product ID
- 69676-0072_2d97d533-ee09-3bf8-e063-6294a90ab895
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Genexa Inc.
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-07-26
- Substance
- CALCIUM CARBONATE
- Active strength
- 1000 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
- Genexa Antacid
- Brand name suffix
- Maximum 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69676-0072-4 | Genexa AntacidMaximum 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 |
|---|
| 69676-0072 | GENEXA ANTACID MAXIMUM STRENGTH (CALCIUM CARBONATE) TABLET, CHEWABLE [GENEXA INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250210_e4b8f068-ad52-10c8-e053-2a95a90a871f.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 |
|---|
| 69676-0072-4 | 69676007204 | 72 TABLET, CHEWABLE in 1 BOTTLE (69676-0072-4) | 2022-07-26 | 0000-00-00 | No | No | Current |