Allergy Relief
- Product NDC
- 37808-741
- 11-digit product format
- 378080741
- Labeler code
- 37808
- Product ID
- 37808-741_65e433e3-7e71-43a0-ae5d-debc18668738
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA207235
- Marketing category
- ANDA
- Marketing start
- 2018-03-31
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-741-25 | 37808074125 | 1 BOTTLE in 1 BOX (37808-741-25) > 25 CAPSULE in 1 BOTTLE | 1 bottle | 2018-03-31 | 0000-00-00 | No | No | Current |