Famotidine
- Product NDC
- 70518-0460
- 11-digit product format
- 705180460
- Labeler code
- 70518
- Product ID
- 70518-0460_e1a5364d-d0ac-f7ca-e053-2995a90aa873
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075511
- Marketing category
- ANDA
- Marketing start
- 2017-04-25
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0460-0 | 70518046000 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0460-0) | 2017-04-25 | 0000-00-00 | No | No | Current |
| 70518-0460-1 | 70518046001 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0460-1) | 2018-04-27 | 0000-00-00 | No | No | Current |