Regular Strength
- Product NDC
- 71399-9939
- 11-digit product format
- 713999939
- Labeler code
- 71399
- Product ID
- 71399-9939_3f7feae3-45bd-adf8-e063-6294a90aee4d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antacid Calcium carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- AKRON PHARMA INC
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-09-23
- Substance
- CALCIUM CARBONATE
- Active strength
- 500 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
- Regular Strength
- Brand name suffix
- Assorted Flavors
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM CARBONATE | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H0G9379FGK |
| Rxcui | 308907 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71399-9939-1 | Regular StrengthAssorted Flavors | 150 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 150 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71399-9939-1 | 71399993901 | 150 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (71399-9939-1) | 2025-09-23 | No | No | Historical |