sunmark childrens all day allergy
- Product NDC
- 49348-934
- 11-digit product format
- 493480934
- Labeler code
- 49348
- Product ID
- 49348-934_18c9ff05-74fd-403e-a494-dceb0667a0f0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA090254
- Marketing category
- ANDA
- Marketing start
- 2010-09-09
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 5 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49348-934-34 | 49348093434 | 1 BOTTLE in 1 CARTON (49348-934-34) > 118 mL in 1 BOTTLE | 1 bottle | 2010-09-09 | 0000-00-00 | No | No | Current |