Hydromorphone Hydrochloride
- Product NDC
- 71335-0233
- 11-digit product format
- 713350233
- Labeler code
- 71335
- Product ID
- 71335-0233_f0b78f98-d632-40a9-a5aa-317ed5d50338
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydromorphone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077471
- Marketing category
- ANDA
- Marketing start
- 2009-12-09
- Marketing end
- 0000-00-00
- Substance
- HYDROMORPHONE HYDROCHLORIDE
- Active strength
- 8 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 71335-0233-1 | 71335023301 | 30 TABLET in 1 BOTTLE (71335-0233-1) | 30 tablet | 2009-12-09 | 0000-00-00 | No | No | Current |
| 71335-0233-2 | 71335023302 | 60 TABLET in 1 BOTTLE (71335-0233-2) | 60 tablet | 2009-12-09 | 0000-00-00 | No | No | Current |
| 71335-0233-3 | 71335023303 | 90 TABLET in 1 BOTTLE (71335-0233-3) | 90 tablet | 2009-12-09 | 0000-00-00 | No | No | Current |
| 71335-0233-4 | 71335023304 | 120 TABLET in 1 BOTTLE (71335-0233-4) | 120 tablet | 2009-12-09 | 0000-00-00 | No | No | Current |
| 71335-0233-5 | 71335023305 | 20 TABLET in 1 BOTTLE (71335-0233-5) | 20 tablet | 2009-12-09 | 0000-00-00 | No | No | Current |