Famotidine
- Product NDC
- 66267-543
- 11-digit product format
- 662670543
- Labeler code
- 66267
- Product ID
- 66267-543_9cbdbe41-133a-6938-e053-2a95a90ae941
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA078916
- Marketing category
- ANDA
- Marketing start
- 2016-01-29
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 20 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66267-543-20 | 66267054320 | 20 TABLET in 1 BOTTLE (66267-543-20) | 20 tablet | 2016-11-15 | 0000-00-00 | No | No | Current |
| 66267-543-60 | 66267054360 | 60 TABLET in 1 BOTTLE (66267-543-60) | 60 tablet | 2016-11-15 | 0000-00-00 | No | No | Current |