ADVIL
- Product NDC
- 29485-6749
- 11-digit product format
- 294856749
- Labeler code
- 29485
- Product ID
- 29485-6749_f2175fae-9ac7-f8c1-e053-2995a90affbd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN Tablet coated
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Mechanical Servants LLC
- Application
- NDA018989
- Marketing category
- NDA
- Marketing start
- 2017-02-06
- Marketing end
- 0000-00-00
- 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
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 29485-6749 | ADVIL (IBUPROFEN TABLET COATED) TABLET, COATED [LIL' DRUG STORE PRODUCTS, INC.] | 9 | Legacy NDC | 20231207_d09ddb5a-465b-519f-e053-2995a90a16d5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 29485-6749-6 | 29485674906 | 3 POUCH in 1 BLISTER PACK (29485-6749-6) > 2 TABLET, COATED in 1 POUCH | 3 pouch | 2017-02-06 | 0000-00-00 | No | No | Current |