Etodolac
- Product NDC
- 50436-0041
- 11-digit product format
- 504360041
- Labeler code
- 50436
- Product ID
- 50436-0041_2be00133-b56c-4d47-8b69-d5bb7626939c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA076004
- Marketing category
- ANDA
- Marketing start
- 2003-05-01
- Marketing end
- 0000-00-00
- Substance
- ETODOLAC
- Active strength
- 400 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 50436-0041-2 | Etodolac | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0041 | ETODOLAC TABLET, FILM COATED [UNIT DOSE SERVICES] | 5 | Legacy NDC, 1 package rows | 20180315_dd44aa6d-8d52-4b4f-99fc-20f3cf28e222.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0041-2 | 50436004102 | 60 in 1 BOTTLE | Historical |