Clonidine Hydrochloride
- Product NDC
- 70518-0898
- 11-digit product format
- 705180898
- Labeler code
- 70518
- Product ID
- 70518-0898_e299845a-8474-5ee4-e053-2995a90ac1f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070974
- Marketing category
- ANDA
- Marketing start
- 2017-12-12
- Marketing end
- 0000-00-00
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0898 | CLONIDINE HYDROCHLORIDE TABLET [REMEDYREPACK INC.] | 17 | Legacy NDC | 20250503_84ef7b29-dd48-43d3-bda8-d6337bc22891.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0898-0 | 70518089800 | 30 TABLET in 1 BLISTER PACK (70518-0898-0) | 30 tablet | 2017-12-12 | 0000-00-00 | No | No | Current |
| 70518-0898-1 | 70518089801 | 50 TABLET in 1 BOTTLE, PLASTIC (70518-0898-1) | 50 tablet | 2019-04-18 | 0000-00-00 | No | No | Current |
| 70518-0898-2 | 70518089802 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0898-2) | 90 tablet | 2019-10-18 | 0000-00-00 | No | No | Current |
| 70518-0898-3 | 70518089803 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-0898-3) | 100 tablet | 2019-11-05 | 0000-00-00 | No | No | Current |
| 70518-0898-4 | 70518089804 | 180 TABLET in 1 BOTTLE, PLASTIC (70518-0898-4) | 180 tablet | 2020-01-07 | 0000-00-00 | No | No | Current |
| 70518-0898-5 | 70518089805 | 100 TABLET in 1 BOTTLE (70518-0898-5) | 100 tablet | 2020-11-13 | 0000-00-00 | No | No | Current |