Nitrofurantoin
- Product NDC
- 0472-1992
- 11-digit product format
- 004721992
- Labeler code
- 0472
- Product ID
- 0472-1992_daa2705a-a5a4-407a-9333-8693d3afe00b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitrofurantoin
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA205180
- Marketing category
- ANDA
- Marketing start
- 2016-10-07
- Marketing end
- 0000-00-00
- Substance
- NITROFURANTOIN
- Active strength
- 25 mg/5mL
- Pharmacologic classes
- Nitrofurans [CS],Nitrofuran Antibacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 0472-1992-08 | 00472199208 | 1 BOTTLE, GLASS in 1 CARTON (0472-1992-08) > 230 mL in 1 BOTTLE, GLASS | 2016-10-07 | 0000-00-00 | No | No | Current |