sunmark all day allergy d
- Product NDC
- 70677-0077
- 11-digit product format
- 706770077
- Labeler code
- 70677
- Product ID
- 70677-0077_6b84f9e8-6aae-45cd-86e5-70c03a834aa6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine hydrochloride, Pseudoephedrine hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA210719
- Marketing category
- ANDA
- Marketing start
- 2020-03-04
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 5 mg/1; mg/1
- 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 |
|---|
| 70677-0077-1 | 70677007701 | 24 BLISTER PACK in 1 CARTON (70677-0077-1) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | 24 blister pack | 2020-03-04 | 0000-00-00 | No | No | Current |