BERKLEY JENSEN
- Product NDC
- 68391-033
- 11-digit product format
- 683910033
- Labeler code
- 68391
- Product ID
- 68391-033_c7eedcbf-3b07-4cd3-937b-c56d7cc5bc57
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ANTACID CALCIUM CARBONATE
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- BJWC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-03-17
- 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
- BERKLEY JENSEN
- 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 |
|---|
| 68391-033-65 | BERKLEY JENSENULTRA STRENGTH | 265 in 1 BOTTLE | TABLET, CHEWABLE | 265 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68391-033 | BERKLEY JENSEN ULTRA STRENGTH (ANTACID CALCIUM CARBONATE) TABLET, CHEWABLE [BJWC] | 1 | Current NDC, 1 package rows | 20250410_c7eedcbf-3b07-4cd3-937b-c56d7cc5bc57.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68391-033-65 | 68391003365 | 265 TABLET, CHEWABLE in 1 BOTTLE (68391-033-65) | 2025-03-17 | No | No | Current |