Famotidine
- Product NDC
- 0363-0036
- 11-digit product format
- 003630036
- Labeler code
- 0363
- Product ID
- 0363-0036_25433b9c-601b-46f9-b6a4-c879fdc1a8cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- ANDA090283
- Marketing category
- ANDA
- Marketing start
- 2013-11-07
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0363-0036-26 | EA - Each | 0363-0036 | fcebce7b-a691-4a96-9d5e-a938991e5299 | 1 | 2014-08-01 |
| 0363-0036-50 | EA - Each | 0363-0036 | 5aa40e72-2a51-45e3-8b75-0b1b623dde7e | 1 | 2014-08-01 |
| 0363-0036-83 | EA - Each | 0363-0036 | c07108db-7bf7-4501-b301-9d251850443d | 1 | 2014-08-01 |