OXAPROZIN
- Product NDC
- 70332-310
- 11-digit product format
- 703320310
- Labeler code
- 70332
- Product ID
- 70332-310_5d135044-6049-180a-e053-2991aa0ab763
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXAPROZIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- California Pharmaceuticals LLC
- Application
- ANDA075855
- Marketing category
- ANDA
- Marketing start
- 2017-07-01
- Marketing end
- 0000-00-00
- Substance
- OXAPROZIN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70332-310-01 | OXAPROZIN | 14 in 1 BOTTLE | TABLET, FILM COATED | 14 | | 3 |
| 70332-310-02 | OXAPROZIN | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70332-310 | OXAPROZIN TABLET, FILM COATED [CALIFORNIA PHARMACEUTICALS LLC] | 3 | Legacy NDC, 2 package rows | 20171103_cb1c0ab4-a102-46fe-b4cf-0a43fd6d91d9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 70332-310-01 | 70332031001 | 14 in 1 BOTTLE | Historical |
| 70332-310-02 | 70332031002 | 60 in 1 BOTTLE | Historical |