Good Sense ibuprofen
- Product NDC
- 0113-0517
- 11-digit product format
- 001130517
- Labeler code
- 0113
- Product ID
- 0113-0517_5cdbfc17-2b55-4c98-b31c-b3a57587c29d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- ANDA077349
- Marketing category
- ANDA
- Marketing start
- 2006-04-27
- Substance
- IBUPROFEN
- Active strength
- 200 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Good Sense ibuprofen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IBUPROFEN | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WK2XYI10QM |
| Rxcui | 310965 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0113-0517-71 | Good Sense ibuprofen | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 5 |
| 0113-0517-71 | Good Sense ibuprofen | 50 in 1 BOTTLE | TABLET, FILM COATED | 50 | | 5 |
| 0113-0517-78 | Good Sense ibuprofen | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 5 |
| 0113-0517-78 | Good Sense ibuprofen | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 5 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| IBUPROFEN | ACTIVE INGREDIENT | WK2XYI10QM | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] | 1 | |
| IBUPROFEN | ACTIVE MOIETY | WK2XYI10QM | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] | 1 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] | 1 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] | 1 | |
| POLYVINYL ALCOHOL | INACTIVE INGREDIENT | 532B59J990 | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] | 1 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L PERRIGO COMPANY] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0113-0517 | GOOD SENSE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L. PERRIGO COMPANY] | 5 | Current NDC, Legacy NDC, 4 package rows | 20230809_aebae4b3-18c8-4ecf-b578-1fe7cc50076b.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 |
|---|
| 0113-0517-71 | 00113051771 | 1 BOTTLE in 1 CARTON (0113-0517-71) / 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2006-04-27 | 0000-00-00 | No | No | Current |
| 0113-0517-78 | 00113051778 | 1 BOTTLE in 1 CARTON (0113-0517-78) / 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2022-03-23 | 0000-00-00 | No | No | Current |