nitrofurantoin macrocrystals
- Product NDC
- 43063-675
- 11-digit product format
- 430630675
- Labeler code
- 43063
- Product ID
- 43063-675_d2b9f182-c33d-c3b0-e053-2a95a90ac5a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nitrofurantoin macrocrystals
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA016620
- Marketing category
- NDA
- Marketing start
- 2010-09-27
- Marketing end
- 0000-00-00
- Substance
- NITROFURANTOIN
- Active strength
- 50 mg/1
- Pharmacologic classes
- Nitrofurans [CS],Nitrofuran Antibacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 43063-675-28 | 43063067528 | 28 CAPSULE in 1 BOTTLE, PLASTIC (43063-675-28) | 28 capsule | 2016-06-09 | 0000-00-00 | No | No | Current |
| 43063-675-40 | 43063067540 | 40 CAPSULE in 1 BOTTLE, PLASTIC (43063-675-40) | 40 capsule | 2016-06-21 | 0000-00-00 | No | No | Current |