clonidine hydrochloride
- Product NDC
- 60760-178
- 11-digit product format
- 607600178
- Labeler code
- 60760
- Product ID
- 60760-178_7a7f80b0-0999-3d7c-e053-2a91aa0aba56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA078895
- Marketing category
- ANDA
- Marketing start
- 2009-09-21
- 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
- 2020-12-31
- 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 |
|---|
| 60760-178-30 | 60760017830 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-178-30) | 30 tablet | 2017-12-15 | 0000-00-00 | No | No | Current |
| 60760-178-90 | 60760017890 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-178-90) | 90 tablet | 2017-12-27 | 0000-00-00 | No | No | Current |