Nizatidine
- Product NDC
- 68071-5043
- 11-digit product format
- 680715043
- Labeler code
- 68071
- Product ID
- 68071-5043_bbb39fd6-4bb0-0b14-e053-2995a90a63aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nizatidine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075616
- Marketing category
- ANDA
- Marketing start
- 2002-07-09
- Marketing end
- 0000-00-00
- Substance
- NIZATIDINE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68071-5043-6 | 68071504306 | 60 CAPSULE in 1 BOTTLE (68071-5043-6) | 60 capsule | 2019-08-28 | 0000-00-00 | No | No | Current |