Genexa Antacid Maximum Strength
- Product NDC
- 84998-0098
- 11-digit product format
- 849980098
- Labeler code
- 84998
- Product ID
- 84998-0098_27fde2d4-4d49-d995-e063-6394a90ad648
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium Carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- PNP Pharmaceuticals Inc
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-31
- 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 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84998-0098-4 | Genexa Antacid Maximum Strength | 72 in 1 BOTTLE | TABLET, CHEWABLE | 72 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 84998-0098-4 | 84998009804 | 72 TABLET, CHEWABLE in 1 BOTTLE (84998-0098-4) | 2025-08-31 | No | No | Historical |