Oxycodone Hydrochloride
- Product NDC
- 72162-1336
- 11-digit product format
- 721621336
- Labeler code
- 72162
- Product ID
- 72162-1336_8791aa09-9719-4998-8f3e-6d9453463ff7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091490
- Marketing category
- ANDA
- Marketing start
- 2014-09-08
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Oxycodone Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXYCODONE HYDROCHLORIDE | 15 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C1ENJ2TE6C |
| Rxcui | 1049611 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1336-1 | Oxycodone Hydrochloride | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 103 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1336 | OXYCODONE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 102 | Current NDC, 1 package rows | 20240727_0e4dd113-87ab-4a5d-846a-446db3cfd469.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1336-1 | 72162133601 | 100 TABLET in 1 BOTTLE, PLASTIC (72162-1336-1) | 100 tablet | 2026-04-07 | No | No | Historical |