Sunmark childrens all day allergy
- Product NDC
- 70677-0015
- 11-digit product format
- 706770015
- Labeler code
- 70677
- Product ID
- 70677-0015_64197bed-0648-48d7-8f17-82e683204bf7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA204226
- Marketing category
- ANDA
- Marketing start
- 2016-10-31
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 5 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 70677-0015-1 | 70677001501 | 1 BOTTLE in 1 CARTON (70677-0015-1) > 118 mL in 1 BOTTLE | 1 bottle | 2016-10-31 | 0000-00-00 | No | No | Current |