EXALGO
- Product NDC
- 23635-432
- 11-digit product format
- 236350432
- Labeler code
- 23635
- Product ID
- 23635-432_0cc967c3-2f93-438b-a25c-0a4bbaf4f313
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydromorphone Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- SpecGx LLC
- Application
- NDA021217
- Marketing category
- NDA
- Marketing start
- 2010-03-01
- Marketing end
- 2021-03-31
- Substance
- HYDROMORPHONE HYDROCHLORIDE
- Active strength
- 32 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 23635-432-01 | 23635043201 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23635-432-01) | 2010-03-01 | 2021-03-31 | No | No | Current |