Nitrofurantoin
- Product NDC
- 60687-472
- 11-digit product format
- 606870472
- Labeler code
- 60687
- Product ID
- 60687-472_ea3cebe3-706d-4e52-e053-2995a90a2918
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitrofurantoin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA201722
- Marketing category
- ANDA
- Marketing start
- 2019-11-18
- Marketing end
- 0000-00-00
- Substance
- NITROFURANTOIN
- Active strength
- 50 mg/1
- Pharmacologic classes
- Nitrofuran Antibacterial [EPC], Nitrofurans [CS]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-472-01 | 60687047201 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-472-01) > 1 CAPSULE in 1 BLISTER PACK (60687-472-11) | 100 blister pack | 2019-10-28 | 0000-00-00 | No | No | Current |