Nitrofurantoin Macrocrystals
- Product NDC
- 50436-6591
- 11-digit product format
- 504366591
- Labeler code
- 50436
- Product ID
- 50436-6591_c10f78f1-d9b1-4843-9162-ee73debee64e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nitrofurantoin Macrocrystals
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA073652
- Marketing category
- ANDA
- Marketing start
- 2007-03-08
- Marketing end
- 0000-00-00
- Substance
- NITROFURANTOIN
- Active strength
- 100 mg/1
- Pharmacologic classes
- Nitrofurans [CS],Nitrofuran Antibacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record