Clonidine Hydrochloride
- Product NDC
- 63739-060
- 11-digit product format
- 637390060
- Labeler code
- 63739
- Product ID
- 63739-060_b3c7f09f-f561-452c-e053-2995a90a7c9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA070974
- Marketing category
- ANDA
- Marketing start
- 1995-01-03
- Marketing end
- 2021-08-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-060-10 | 63739006010 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-060-10) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 1995-01-03 | 2021-08-31 | No | No | Current |