OXYCODONE HYDROCHLORIDE
- Product NDC
- 71335-0209
- 11-digit product format
- 713350209
- Labeler code
- 71335
- Product ID
- 71335-0209_cdf8c60b-28ff-4c8d-b9c1-48c59ad0ae0d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYCODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077290
- Marketing category
- ANDA
- Marketing start
- 2012-12-26
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 30 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 |
|---|
| 71335-0209-1 | 71335020901 | 60 TABLET in 1 BOTTLE (71335-0209-1) | 60 tablet | 2015-05-28 | 0000-00-00 | No | No | Current |
| 71335-0209-2 | 71335020902 | 90 TABLET in 1 BOTTLE (71335-0209-2) | 90 tablet | 2015-05-28 | 0000-00-00 | No | No | Current |
| 71335-0209-3 | 71335020903 | 120 TABLET in 1 BOTTLE (71335-0209-3) | 120 tablet | 2015-05-28 | 0000-00-00 | No | No | Current |
| 71335-0209-4 | 71335020904 | 30 TABLET in 1 BOTTLE (71335-0209-4) | 30 tablet | 2015-05-28 | 0000-00-00 | No | No | Current |
| 71335-0209-5 | 71335020905 | 100 TABLET in 1 BOTTLE (71335-0209-5) | 100 tablet | 2015-05-28 | 0000-00-00 | No | No | Current |
| 71335-0209-6 | 71335020906 | 40 TABLET in 1 BOTTLE (71335-0209-6) | 40 tablet | 2015-05-28 | 0000-00-00 | No | No | Current |
| 71335-0209-7 | 71335020907 | 18 TABLET in 1 BOTTLE (71335-0209-7) | 18 tablet | 2015-05-28 | 0000-00-00 | No | No | Current |
| 71335-0209-8 | 71335020908 | 28 TABLET in 1 BOTTLE (71335-0209-8) | 28 tablet | 2015-05-28 | 0000-00-00 | No | No | Current |