Oxaprozin
- Product NDC
- 63629-8724
- 11-digit product format
- 636298724
- Labeler code
- 63629
- Product ID
- 63629-8724_1dc2d61f-6958-4e0c-b4b4-ae659eb86e83
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxaprozin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075845
- Marketing category
- ANDA
- Marketing start
- 2001-01-31
- Substance
- OXAPROZIN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-8724-1 | Oxaprozin | 100 in 1 BOTTLE | TABLET | 100 | | 103 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-8724 | OXAPROZIN TABLET [BRYANT RANCH PREPACK] | 103 | Current NDC, Legacy NDC, 1 package rows | 20231102_42f56cc8-9843-4786-9bc6-5699a06676be.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8724-1 | 63629872401 | 100 TABLET in 1 BOTTLE (63629-8724-1) | 100 tablet | 2021-08-19 | 0000-00-00 | No | No | Current |