assorted fruit antacid flavor chews
- Product NDC
- 36800-828
- Requested package NDC
- 36800-828-36
- 11-digit product format
- 368000828
- Labeler code
- 36800
- Product ID
- 36800-828_edadb834-86b6-e022-e053-2a95a90a2cdb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- calcium carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Topco Associates
- Application
- part331
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-06-01
- 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 | 36800-828 | 36800-828-36 | D | Discontinued by firm | 2026-10-15 |
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 |
|---|---|---|---|---|---|---|---|
| 36800-828-36 | 36800082836 | 36 TABLET, CHEWABLE in 1 BOTTLE (36800-828-36) | 2015-06-01 | 0000-00-00 | No | No | Current |