OXYCODONE HYDROCHLORIDE
- Product NDC
- 60760-955
- Requested package NDC
- 60760-955-60
- 11-digit product format
- 607600955
- Labeler code
- 60760
- Product ID
- 60760-955_3cd0143b-2802-e698-e063-6294a90aa581
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYCODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA091393
- Marketing category
- ANDA
- Marketing start
- 2013-10-18
- 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
- 2026-12-31
- Current FDA listing
- Yes
Orange Book products#
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| A091393-001 | OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | 5MG | TABLET / ORAL | AB | 2009-08-31 | |
| A091393-002 | OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | 10MG | TABLET / ORAL | AB | RS | 2009-08-31 |
| A091393-003 | OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | 15MG | TABLET / ORAL | AB | 2009-08-31 | |
| A091393-004 | OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | 20MG | TABLET / ORAL | AB | 2009-08-31 | |
| A091393-005 | OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | 30MG | TABLET / ORAL | AB | 2009-08-31 |
Therapeutic equivalence codes#
| Application-product | TE code |
|---|---|
| A091393-001 | AB |
| A091393-002 | AB |
| A091393-003 | AB |
| A091393-004 | AB |
| A091393-005 | AB |
Observed Orange Book product history#
Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-08-01 22:54:32 | 2026-06 | A091393-001 | OXYCODONE HYDROCHLORIDE | 5MG | TABLET / ORAL | AB | 2009-08-31 | a50c72e98297… | |
| 2026-08-01 22:54:32 | 2026-06 | A091393-002 | OXYCODONE HYDROCHLORIDE | 10MG | TABLET / ORAL | AB | RS | 2009-08-31 | a50c72e98297… |
| 2026-08-01 22:54:32 | 2026-06 | A091393-003 | OXYCODONE HYDROCHLORIDE | 15MG | TABLET / ORAL | AB | 2009-08-31 | a50c72e98297… | |
| 2026-08-01 22:54:32 | 2026-06 | A091393-004 | OXYCODONE HYDROCHLORIDE | 20MG | TABLET / ORAL | AB | 2009-08-31 | a50c72e98297… | |
| 2026-08-01 22:54:32 | 2026-06 | A091393-005 | OXYCODONE HYDROCHLORIDE | 30MG | TABLET / ORAL | AB | 2009-08-31 | a50c72e98297… |
Observed Orange Book normalized TE history#
| Captured | Edition | Application-product | TE code | Order | Source SHA-256 |
|---|---|---|---|---|---|
| 2026-08-01 22:54:32 | 2026-06 | A091393-001 | AB | 1 | a50c72e98297… |
| 2026-08-01 22:54:32 | 2026-06 | A091393-002 | AB | 1 | a50c72e98297… |
| 2026-08-01 22:54:32 | 2026-06 | A091393-003 | AB | 1 | a50c72e98297… |
| 2026-08-01 22:54:32 | 2026-06 | A091393-004 | AB | 1 | a50c72e98297… |
| 2026-08-01 22:54:32 | 2026-06 | A091393-005 | AB | 1 | a50c72e98297… |
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | St. Mary's Medical Park Pharmacy | 3ccf459a-fb11-e137-e063-6394a90a5a80 | 2026-07-14 | Boxed warning, Warnings, Adverse reactions | 091393 ANDA091393 |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | Bryant Ranch Prepack | 685d9709-028e-4422-bf0c-fde577b718a2 | 2026-07-14 | Boxed warning, Warnings, Adverse reactions | 091393 ANDA091393 |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | KVK-TECH,INC | e73897d6-b920-4300-a564-5dbc9c8e9fe9 | 2026-06-04 | Boxed warning, Warnings, Adverse reactions | 091393 ANDA091393 |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | ST. MARY'S MEDICAL PARK PHARMACY | 424fdfc7-1c92-2e62-e063-6394a90a136b | 2026-05-19 | Boxed warning, Warnings, Adverse reactions | 091393 ANDA091393 |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | American Health Packaging | aa7ac2bf-d9ed-445d-b394-4d3fe39780ca | 2025-10-17 | Boxed warning, Warnings, Adverse reactions | 091393 ANDA091393 |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | ST. MARY'S MEDICAL PARK PHARMACY | 3cd01fb7-b59c-fc5d-e063-6394a90a21d2 | 2025-08-20 | Boxed warning, Warnings, Adverse reactions | 091393 ANDA091393 60760-955-60 60760-955 60760095560 |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | DIRECT RX | a8206207-ad09-83df-e053-2995a90a78b7 | 2025-06-05 | Boxed warning, Warnings, Adverse reactions | 091393 ANDA091393 |
| Oxycodone HCL | OXYCODONE HCL | Direct_Rx | 31189587-a2dc-e0a1-e063-6394a90ae17d | 2025-03-24 | Boxed warning, Warnings, Adverse reactions | 091393 ANDA091393 |
| Oxycodone Hydchloride | OXYCODONE HYDCHLORIDE | Quality Care Products LLC | b9847cc7-67a2-408d-93cf-f9cf420346dd | 2024-12-19 | Warnings, Adverse reactions | 091393 ANDA091393 |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | Quality Care Products LLC | 4cadb809-157d-49cc-97b4-3276594f19d2 | 2024-12-19 | Warnings, Adverse reactions | 091393 ANDA091393 |
| Oxycodone Hydchloride | OXYCODONE HYDCHLORIDE | Quality Care Products LLC | 28156b13-0ba9-4dc4-be24-9c3070a7e1cc | 2024-12-16 | Warnings, Adverse reactions | 091393 ANDA091393 |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | NuCare Pharmaceuticals,Inc. | 17f7946d-e889-b736-e063-6394a90a42e0 | 2024-05-08 | Boxed warning, Warnings, Adverse reactions | 091393 ANDA091393 |
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- OXYCODONE HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| OXYCODONE HYDROCHLORIDE | 10 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| C1ENJ2TE6C | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1049683 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3cd01fb7-b59c-fc5d-e063-6394a90a21d2 | Available on FDA.report |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 60760-955-30 | OXYCODONE HYDROCHLORIDE | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | 1 | |
| 60760-955-60 | OXYCODONE HYDROCHLORIDE | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 60760-955-30 | EA - Each | 60760-955 | 788af49b-98e3-48a0-a74e-d71f538bf03a | 1 | 2025-09-12 |
| 60760-955-60 | EA - Each | 60760-955 | 8da0aea7-06d0-4040-9863-5ae7e0164a65 | 1 | 2025-09-12 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1049683 | oxyCODONE HCl 10 MG Oral Tablet | PSN | 3cd01fb7-b59c-fc5d-e063-6394a90a21d2 | 1 |
| 1049683 | oxycodone hydrochloride 10 MG Oral Tablet | SCD | 3cd01fb7-b59c-fc5d-e063-6394a90a21d2 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 60760-955-60 | 60760095560 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-955-60) | 60 tablet | 2025-08-20 | No | No | Current |