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- Product NDC
- 63940-458
- 11-digit product format
- 639400458
- Labeler code
- 63940
- Product ID
- 63940-458_68b14f2a-1664-4042-8c17-de93b5fbefb1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Harmon Stores Inc.
- Application
- ANDA078336
- Marketing category
- ANDA
- Marketing start
- 2011-12-18
- 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 |
|---|---|---|---|---|---|---|---|---|
| 63940-458-39 | 63940045839 | 1 BOTTLE in 1 CARTON (63940-458-39) > 30 TABLET in 1 BOTTLE | 1 bottle | 2011-12-18 | 0000-00-00 | No | No | Current |
| 63940-458-66 | 63940045866 | 14 BLISTER PACK in 1 CARTON (63940-458-66) > 1 TABLET in 1 BLISTER PACK | 14 blister pack | 2011-12-18 | 0000-00-00 | No | No | Current |