Rx Act all day allergy relief
- Product NDC
- 37808-458
- 11-digit product format
- 378080458
- Labeler code
- 37808
- Product ID
- 37808-458_7a07a7c9-a4ec-408c-8560-db8fe5b713a9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA078336
- Marketing category
- ANDA
- Marketing start
- 2008-01-31
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 37808-458-39 | 2020-12-18 | C162847 | 48780-1 | 9d75b9d0-6b1a-f424-e053-dadaa90a57ce | 9a51b7df-2e98-41c4-9ca5-efd50d50fbb6 |
| 37808-458-66 | 2020-12-18 | C162847 | 48780-1 | 9d75b9d0-6b1a-f424-e053-dadaa90a57ce | 9a51b7df-2e98-41c4-9ca5-efd50d50fbb6 |
| 37808-458-72 | 2020-12-18 | C162847 | 48780-1 | 9d75b9d0-6b1a-f424-e053-dadaa90a57ce | 9a51b7df-2e98-41c4-9ca5-efd50d50fbb6 |
| 37808-458-76 | 2020-12-18 | C162847 | 48780-1 | 9d75b9d0-6b1a-f424-e053-dadaa90a57ce | 9a51b7df-2e98-41c4-9ca5-efd50d50fbb6 |
| 37808-458-39 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-6b1a-f424-e053-dadaa90a57ce | 9a51b7df-2e98-41c4-9ca5-efd50d50fbb6 |
| 37808-458-66 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-6b1a-f424-e053-dadaa90a57ce | 9a51b7df-2e98-41c4-9ca5-efd50d50fbb6 |
| 37808-458-72 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-6b1a-f424-e053-dadaa90a57ce | 9a51b7df-2e98-41c4-9ca5-efd50d50fbb6 |
| 37808-458-76 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-6b1a-f424-e053-dadaa90a57ce | 9a51b7df-2e98-41c4-9ca5-efd50d50fbb6 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 37808-458-76 | EA - Each | 37808-458 | 1946113d-3275-4aa2-869d-966f7bafee6c | 1 | 2022-06-06 |