FLONASE
- Product NDC
- 0135-1329
- 11-digit product format
- 001351329
- Labeler code
- 0135
- Product ID
- 0135-1329_070fb5a4-1848-41e8-90bf-57e682de1762
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- triprolidine hcl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-12-15
- Marketing end
- 0000-00-00
- Substance
- TRIPROLIDINE HYDROCHLORIDE
- Active strength
- 3 mg/1
- 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 product | product | 0135-1329 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 0135-1329 | 0135-1329-01 | D | Discontinued by firm | 2026-10-05 |
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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0135-1329-01 | 00135132901 | 1 BLISTER PACK in 1 CARTON (0135-1329-01) > 36 TABLET in 1 BLISTER PACK | 1 blister pack | 2022-12-15 | 0000-00-00 | No | No | Current |