Famotidine
- Product NDC
- 68071-3305
- 11-digit product format
- 680713305
- Labeler code
- 68071
- Product ID
- 68071-3305_bb2b3c0a-6720-4030-e053-2a95a90ac206
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceutical, Inc.
- Application
- ANDA078916
- Marketing category
- ANDA
- Marketing start
- 2016-01-29
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 40 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 |
|---|
| 68071-3305-3 | 68071330503 | 30 TABLET in 1 BOTTLE (68071-3305-3) | 30 tablet | 2017-05-25 | 0000-00-00 | No | No | Current |
| 68071-3305-6 | 68071330506 | 60 TABLET in 1 BOTTLE (68071-3305-6) | 60 tablet | 2017-05-25 | 0000-00-00 | No | No | Current |
| 68071-3305-9 | 68071330509 | 90 TABLET in 1 BOTTLE (68071-3305-9) | 90 tablet | 2017-05-25 | 0000-00-00 | No | No | Current |