Oxycodone Hydrochloride
- Product NDC
- 63629-4184
- 11-digit product format
- 636294184
- Labeler code
- 63629
- Product ID
- 63629-4184_dbc5254f-4f73-49ee-a8af-b3280963a05a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077712
- Marketing category
- ANDA
- Marketing start
- 2009-03-02
- 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
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63629-4184-1 | EA - Each | 63629-4184 | a56e1177-bae4-4e65-9606-6b433730600e | 1 | 2012-07-24 |
| 63629-4184-2 | EA - Each | 63629-4184 | 828efece-7773-4e64-b0a2-300e40cf7abc | 1 | 2012-07-24 |
| 63629-4184-3 | EA - Each | 63629-4184 | 3af67f53-e4ba-49b5-933a-9093e160c278 | 1 | 2012-07-24 |
| 63629-4184-4 | EA - Each | 63629-4184 | 6a25ebb4-02c0-4490-bb9c-8d0876cbf47c | 1 | 2012-07-24 |
| 63629-4184-5 | EA - Each | 63629-4184 | 3360a49c-4603-4c4c-bfb2-1bdd8d3952dc | 1 | 2012-07-24 |
| 63629-4184-6 | EA - Each | 63629-4184 | b8751d76-6e4e-4087-92e9-9dec642a0476 | 1 | 2013-02-13 |
| 63629-4184-7 | EA - Each | 63629-4184 | 762172d9-71d6-4c79-abb8-cf984f0400e3 | 1 | 2013-02-13 |
| 63629-4184-8 | EA - Each | 63629-4184 | 453a7662-e79c-4950-9b09-3661bcb0824a | 1 | 2013-02-13 |