Famotidine
- Product NDC
- 68071-1879
- 11-digit product format
- 680711879
- Labeler code
- 68071
- Product ID
- 68071-1879_4041d4de-40fe-292e-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA206530
- Marketing category
- ANDA
- Marketing start
- 2015-12-22
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68071-1879-3 | 2020-06-26 | C162847 | 48780-1 | 9d75b9d0-61c9-f424-e053-dadaa90a57ce | 4041eb22-b373-2d46-e054-00144ff8d46c |
| 68071-1879-6 | 2020-06-26 | C162847 | 48780-1 | 9d75b9d0-61c9-f424-e053-dadaa90a57ce | 4041eb22-b373-2d46-e054-00144ff8d46c |
| 68071-1879-9 | 2020-06-26 | C162847 | 48780-1 | 9d75b9d0-61c9-f424-e053-dadaa90a57ce | 4041eb22-b373-2d46-e054-00144ff8d46c |
| 68071-1879-3 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-61c9-f424-e053-dadaa90a57ce | 4041eb22-b373-2d46-e054-00144ff8d46c |
| 68071-1879-6 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-61c9-f424-e053-dadaa90a57ce | 4041eb22-b373-2d46-e054-00144ff8d46c |
| 68071-1879-9 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-61c9-f424-e053-dadaa90a57ce | 4041eb22-b373-2d46-e054-00144ff8d46c |