OXYCODONE HYDROCHLORIDE
- Product NDC
- 63629-3775
- 11-digit product format
- 636293775
- Labeler code
- 63629
- Product ID
- 63629-3775_8cd841f7-9420-417f-9814-04dcb9b48737
- 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
- 10 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-3775-1 | 63629377501 | 90 TABLET in 1 BOTTLE (63629-3775-1) | 90 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |
| 63629-3775-2 | 63629377502 | 60 TABLET in 1 BOTTLE (63629-3775-2) | 60 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |
| 63629-3775-3 | 63629377503 | 120 TABLET in 1 BOTTLE (63629-3775-3) | 120 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |
| 63629-3775-4 | 63629377504 | 10 TABLET in 1 BOTTLE (63629-3775-4) | 10 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |
| 63629-3775-5 | 63629377505 | 30 TABLET in 1 BOTTLE (63629-3775-5) | 30 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |
| 63629-3775-6 | 63629377506 | 20 TABLET in 1 BOTTLE (63629-3775-6) | 20 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |