Nizatidine
- Product NDC
- 63629-2769
- 11-digit product format
- 636292769
- Labeler code
- 63629
- Product ID
- 63629-2769_8a317b5d-3e0a-4eee-8f42-b0950dba5f52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nizatidine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077314
- Marketing category
- ANDA
- Marketing start
- 2005-09-15
- Marketing end
- 0000-00-00
- Substance
- NIZATIDINE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2769-1 | 63629276901 | 60 CAPSULE in 1 BOTTLE (63629-2769-1) | 60 capsule | 2019-01-01 | 0000-00-00 | No | No | Current |
| 63629-2769-2 | 63629276902 | 30 CAPSULE in 1 BOTTLE (63629-2769-2) | 30 capsule | 2019-01-01 | 0000-00-00 | No | No | Current |