oxycodone and acetaminophen
- Product NDC
- 55700-658
- 11-digit product format
- 557000658
- Labeler code
- 55700
- Product ID
- 55700-658_2783ad86-5a26-412d-8f9f-da2e084d8934
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxycodone and acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA090535
- Marketing category
- ANDA
- Marketing start
- 2018-07-20
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|---|---|---|---|---|
| 55700-658-01 | EA - Each | 55700-658 | 2e984de2-8684-42d4-a140-751fce1a9df6 | 1 | 2018-08-13 |
| 55700-658-14 | EA - Each | 55700-658 | 76ee262d-04ed-444e-a96a-9f40ca25b324 | 1 | 2018-10-11 |
| 55700-658-15 | EA - Each | 55700-658 | 3a26b7e0-e99e-4411-a8c8-79199c0b957e | 1 | 2018-08-13 |
| 55700-658-20 | EA - Each | 55700-658 | 7cc2cf32-a613-4b77-ad67-9ff937f48d92 | 1 | 2018-08-13 |
| 55700-658-21 | EA - Each | 55700-658 | b0e63e83-08db-4c37-a780-44c890506a66 | 1 | 2018-11-06 |
| 55700-658-24 | EA - Each | 55700-658 | 23cb8a62-0ecb-467d-9dbd-7ef1eb834416 | 1 | 2018-08-13 |
| 55700-658-30 | EA - Each | 55700-658 | bc3f6e11-d98c-452d-a330-4f372b4520fe | 1 | 2018-08-13 |
| 55700-658-40 | EA - Each | 55700-658 | fb6d26bd-66b8-48cd-a28a-a84ab74c3119 | 1 | 2018-08-13 |
| 55700-658-56 | EA - Each | 55700-658 | ca4c23e8-0617-42f4-bd4d-9c71201f00e7 | 1 | 2018-09-05 |
| 55700-658-60 | EA - Each | 55700-658 | 8d15f462-3a6a-4521-aa15-0a9fed77c7e5 | 1 | 2018-08-13 |
| 55700-658-90 | EA - Each | 55700-658 | 75f8a63d-f672-4603-b219-b2a0a226801b | 1 | 2018-08-13 |