Basic Care All Day Allergy
- Product NDC
- 0113-7002
- 11-digit product format
- 001137002
- Labeler code
- 0113
- Product ID
- 0113-7002_8a4a8453-7dea-4e4a-8536-cdc4d08fed5f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- ANDA078336
- Marketing category
- ANDA
- Marketing start
- 2017-08-08
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0113-7002-75 | 00113700275 | 1 BOTTLE in 1 CARTON (0113-7002-75) > 90 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-08-08 | 0000-00-00 | No | No | Current |
| 0113-7002-87 | 00113700287 | 1 BOTTLE in 1 CARTON (0113-7002-87) > 300 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-08-16 | 0000-00-00 | No | No | Current |