Indomethacin
- Product NDC
- 0409-1113
- 11-digit product format
- 004091113
- Labeler code
- 0409
- Product ID
- 0409-1113_56cfd67e-daf1-4bff-989f-8080555a1bb3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Indomethacin
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- ANDA204118
- Marketing category
- ANDA
- Marketing start
- 2017-01-31
- Marketing end
- 0000-00-00
- Substance
- INDOMETHACIN SODIUM
- Active strength
- 1 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
- 2023-12-31
- 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 |
|---|
| 0409-1113-01 | 00409111301 | 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1113-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE | 2017-01-31 | 0000-00-00 | No | No | Current |