Extra Strength
- Product NDC
- 21130-203
- 11-digit product format
- 211300203
- Labeler code
- 21130
- Product ID
- 21130-203_4249d15f-ba1a-9084-e063-6294a90a391b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antacid Tablets
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- SAFEWAY
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-10-05
- Substance
- CALCIUM CARBONATE
- Active strength
- 750 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
- Extra Strength
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM CARBONATE | 750 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H0G9379FGK |
| Rxcui | 308915 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21130-203-96 | Extra Strength | 96 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 96 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-203 | EXTRA STRENGTH (ANTACID TABLETS) TABLET, CHEWABLE [SAFEWAY] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241102_f91aa7da-8bdc-4fd2-a9de-fef21674e515.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 |
|---|
| 21130-203-96 | 21130020396 | 96 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (21130-203-96) | 2020-10-05 | 0000-00-00 | No | No | Current |