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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0135-1329 | FLONASE NIGHTTIME ALLERGY RELIEF (TRIPROLIDINE HCL) TABLET [HALEON US HOLDINGS LLC] | 4 | Legacy NDC | 20241004_070fb5a4-1848-41e8-90bf-57e682de1762.zip |
Packages#
Package NDC, 11-digit format, Description table| 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 |