Clonidine Hydrochloride
- Product NDC
- 70518-1959
- 11-digit product format
- 705181959
- Labeler code
- 70518
- Product ID
- 70518-1959_eac401e9-e81b-ef88-e053-2a95a90aba7e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA070975
- Marketing category
- ANDA
- Marketing start
- 2019-03-14
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1959-0 | 70518195900 | 30 TABLET in 1 BLISTER PACK (70518-1959-0) | 30 tablet | 2019-03-14 | 0000-00-00 | No | No | Current |
| 70518-1959-1 | 70518195901 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1959-1) | 90 tablet | 2019-09-06 | 0000-00-00 | No | No | Current |