Etodolac
- Product NDC
- 60760-281
- 11-digit product format
- 607600281
- Labeler code
- 60760
- Product ID
- 60760-281_7a8e2c72-4d45-2680-e053-2991aa0a73d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etodolac
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA091134
- Marketing category
- ANDA
- Marketing start
- 2018-02-14
- Marketing end
- 0000-00-00
- Substance
- ETODOLAC
- Active strength
- 600 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-281-15 | 60760028115 | 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-281-15) | 2018-02-14 | 0000-00-00 | No | No | Current |
| 60760-281-30 | 60760028130 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-281-30) | 2018-02-14 | 0000-00-00 | No | No | Current |