Cetirizine HCl
- Product NDC
- 49738-211
- 11-digit product format
- 497380211
- Labeler code
- 49738
- Product ID
- 49738-211_e9483533-e157-4540-bb6b-6093eac283b2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- SMART SENSE (Kmart)
- Application
- NDA022429
- Marketing category
- NDA
- Marketing start
- 2013-05-01
- Marketing end
- 2021-12-31
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49738-211-12 | 49738021112 | 1 BOTTLE, PLASTIC in 1 BOX (49738-211-12) > 12 CAPSULE in 1 BOTTLE, PLASTIC | 2013-05-01 | 2021-12-31 | No | No | Current |
| 49738-211-25 | 49738021125 | 1 BOTTLE, PLASTIC in 1 PACKAGE (49738-211-25) > 25 CAPSULE in 1 BOTTLE, PLASTIC | 2013-05-01 | 2021-12-31 | No | No | Current |