FAMOTIDINE
- Product NDC
- 16714-244
- 11-digit product format
- 167140244
- Labeler code
- 16714
- Product ID
- 16714-244_ffd93549-95d1-4e0e-9572-59f74325d60c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FAMOTIDINE
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA091020
- Marketing category
- ANDA
- Marketing start
- 2021-07-12
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 40 mg/5mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-244-01 | 16714024401 | 50 mL in 1 BOTTLE, PLASTIC (16714-244-01) | 50 ml | 2021-07-12 | 0000-00-00 | No | No | Current |