CVS Ibuprofen Sodium
- Product NDC
- 69842-835
- 11-digit product format
- 698420835
- Labeler code
- 69842
- Product ID
- 69842-835_3323858a-89b5-459b-8d5a-dcb38e458a2b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA206581
- Marketing category
- ANDA
- Marketing start
- 2017-01-10
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN SODIUM
- Active strength
- 256 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 69842-835 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 69842-835 | 69842-835-27 | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 69842-835 | 69842-835-60 | D | Discontinued by firm | | 2026-07-31 |
Orange Book products#
Application-product, Trade name, Ingredient table| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|
| A206581-001 | IBUPROFEN SODIUM | IBUPROFEN SODIUM | EQ 200MG BASE | TABLET / ORAL | | | 2015-08-03 |