Non Drowsy Loratadine
- Product NDC
- 69842-273
- 11-digit product format
- 698420273
- Labeler code
- 69842
- Product ID
- 69842-273_e51e2aec-253d-41b5-a23d-5a9d3cde61f2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA209094
- Marketing category
- ANDA
- Marketing start
- 2020-01-31
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded product | product | 69842-273 | I | Inactivated by FDA | excluded / ndc_excluded.zip | e2bbac7714bc… | 27bdfed8d636… | ||
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded package | package | 69842-273 | 69842-273-10 | I | Inactivated by FDA | excluded / ndc_excluded.zip | e2bbac7714bc… | 27bdfed8d636… | |
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded package | package | 69842-273 | 69842-273-30 | I | Inactivated by FDA | excluded / ndc_excluded.zip | e2bbac7714bc… | 27bdfed8d636… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.