oxycodone hydrochloride
- Product NDC
- 63629-4155
- 11-digit product format
- 636294155
- Labeler code
- 63629
- Product ID
- 63629-4155_4f92eca1-edf5-4b22-a66e-69c549dda71f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxycodone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- bryant ranch prepack
- Application
- ANDA077712
- Marketing category
- ANDA
- Marketing start
- 2010-03-08
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63629-4155-1 | 2021-11-17 | C162847 | 48780-1 | 9855d018-e510-cd31-e053-dbdaa90ab51a | 9ee2fa21-b80d-449a-8e36-260cc79ef600 |
| 63629-4155-2 | 2021-11-17 | C162847 | 48780-1 | 9855d018-e510-cd31-e053-dbdaa90ab51a | 9ee2fa21-b80d-449a-8e36-260cc79ef600 |
| 63629-4155-3 | 2021-11-17 | C162847 | 48780-1 | 9855d018-e510-cd31-e053-dbdaa90ab51a | 9ee2fa21-b80d-449a-8e36-260cc79ef600 |
| 63629-4155-4 | 2021-11-17 | C162847 | 48780-1 | 9855d018-e510-cd31-e053-dbdaa90ab51a | 9ee2fa21-b80d-449a-8e36-260cc79ef600 |
| 63629-4155-1 | 2019-11-27 | C162847 | 48780-1 | 9855d018-e510-cd31-e053-dbdaa90ab51a | 9ee2fa21-b80d-449a-8e36-260cc79ef600 |
| 63629-4155-2 | 2019-11-27 | C162847 | 48780-1 | 9855d018-e510-cd31-e053-dbdaa90ab51a | 9ee2fa21-b80d-449a-8e36-260cc79ef600 |
| 63629-4155-3 | 2019-11-27 | C162847 | 48780-1 | 9855d018-e510-cd31-e053-dbdaa90ab51a | 9ee2fa21-b80d-449a-8e36-260cc79ef600 |
| 63629-4155-4 | 2019-11-27 | C162847 | 48780-1 | 9855d018-e510-cd31-e053-dbdaa90ab51a | 9ee2fa21-b80d-449a-8e36-260cc79ef600 |