FAMOTIDINE
- Product NDC
- 43602-502
- 11-digit product format
- 436020502
- Labeler code
- 43602
- Product ID
- 43602-502_979f9de7-3cc6-4f7f-aaed-96ee208606b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Ascent Pharmaceuticals, Inc.
- Application
- ANDA215689
- Marketing category
- ANDA
- Marketing start
- 2021-10-15
- 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
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43602-502 | FAMOTIDINE TABLET, FILM COATED [ASCENT PHARMACEUTICALS, INC.] | 1 | Legacy NDC | 20211027_3bc583e9-a4b0-4941-9d1c-3521d49a37ef.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43602-502-05 | 43602050205 | 500 TABLET, FILM COATED in 1 BOTTLE (43602-502-05) | 2021-10-15 | 0000-00-00 | No | No | Current |
| 43602-502-30 | 43602050230 | 30 TABLET, FILM COATED in 1 BOTTLE (43602-502-30) | 2021-10-15 | 0000-00-00 | No | No | Current |