Famotidine
- Product NDC
- 68001-240
- 11-digit product format
- 680010240
- Labeler code
- 68001
- Product ID
- 68001-240_c6ea69c0-d43f-68ee-e053-2a95a90ac205
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA078916
- Marketing category
- ANDA
- Marketing start
- 2016-01-29
- Marketing end
- 2022-05-31
- 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
- 0000-00-00
- 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 |
|---|
| 68001-240-00 | 68001024000 | 100 TABLET in 1 BOTTLE (68001-240-00) | 100 tablet | 2016-01-29 | 2022-05-31 | No | No | Current |
| 68001-240-08 | 68001024008 | 1000 TABLET in 1 BOTTLE (68001-240-08) | 1000 tablet | 2016-01-29 | 2022-05-31 | No | No | Current |