Daypro
- Product NDC
- 0025-1381
- 11-digit product format
- 000251381
- Labeler code
- 0025
- Product ID
- 0025-1381_b2dd3c39-1c89-470f-b43b-0c85ed1a2fe1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxaprozin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Application
- NDA018841
- Marketing category
- NDA
- Marketing start
- 1992-10-29
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| OXAPROZIN | ACTIVE INGREDIENT | MHJ80W9LRB | DAYPRO (OXAPROZIN) TABLET, FILM COATED [G.D. SEARLE LLC DIVISION OF PFIZER INC] | 9 | |
| OXAPROZIN | ACTIVE MOIETY | MHJ80W9LRB | DAYPRO (OXAPROZIN) TABLET, FILM COATED [G.D. SEARLE LLC DIVISION OF PFIZER INC] | 9 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | DAYPRO (OXAPROZIN) TABLET, FILM COATED [G.D. SEARLE LLC DIVISION OF PFIZER INC] | 9 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | DAYPRO (OXAPROZIN) TABLET, FILM COATED [G.D. SEARLE LLC DIVISION OF PFIZER INC] | 9 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | DAYPRO (OXAPROZIN) TABLET, FILM COATED [G.D. SEARLE LLC DIVISION OF PFIZER INC] | 9 | |
| METHYLCELLULOSE (100 MPA.S) | INACTIVE INGREDIENT | 4GFU244C4J | DAYPRO (OXAPROZIN) TABLET, FILM COATED [G.D. SEARLE LLC DIVISION OF PFIZER INC] | 9 | |
| POLACRILIN POTASSIUM | INACTIVE INGREDIENT | 0BZ5A00FQU | DAYPRO (OXAPROZIN) TABLET, FILM COATED [G.D. SEARLE LLC DIVISION OF PFIZER INC] | 9 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | DAYPRO (OXAPROZIN) TABLET, FILM COATED [G.D. SEARLE LLC DIVISION OF PFIZER INC] | 9 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | DAYPRO (OXAPROZIN) TABLET, FILM COATED [G.D. SEARLE LLC DIVISION OF PFIZER INC] | 9 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0025-1381 | DAYPRO (OXAPROZIN) TABLET, FILM COATED [PFIZER LABORATORIES DIV PFIZER INC] | 23 | Legacy NDC | 20250124_ea1de47e-3101-4414-817c-0a098af8988c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0025-1381-31 | 00025138131 | 100 TABLET, FILM COATED in 1 BOTTLE (0025-1381-31) | 1992-10-29 | 0000-00-00 | No | No | Current |
| 0025-1381-34 | 00025138134 | 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0025-1381-34) | 1992-10-29 | 0000-00-00 | No | No | Current |
| 0025-1381-51 | 00025138151 | 500 TABLET, FILM COATED in 1 BOTTLE (0025-1381-51) | 1992-10-29 | 0000-00-00 | No | No | Current |