Antacid Flavor Chew
- Product NDC
- 52642-034
- Requested package NDC
- 52642-034-90
- 11-digit product format
- 526420034
- Labeler code
- 52642
- Product ID
- 52642-034_edc647ec-2654-712f-e053-2995a90a0b4c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium Carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- BestCo Inc.
- Application
- part331
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-07-26
- Marketing end
- 0000-00-00
- Substance
- CALCIUM CARBONATE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 52642-034 | 52642-034-90 | D | Discontinued by firm | 2026-10-12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 52642-034-90 | 52642003490 | 90 TABLET, CHEWABLE in 1 BOTTLE (52642-034-90) | 2017-07-26 | 0000-00-00 | No | No | Current |