basic care acid reducer
- Product NDC
- 72288-329
- 11-digit product format
- 722880329
- Labeler code
- 72288
- Product ID
- 72288-329_0829b878-8bb7-4881-b22b-c51c7c027f5c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Amazon.com Services LLC
- Application
- ANDA077351
- Marketing category
- ANDA
- Marketing start
- 2022-01-06
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5QZO15J2Z8 | FAMOTIDINE | 76824-35-6 | FAMOTIDINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72288-329-78 | 72288032978 | 1 BOTTLE in 1 CARTON (72288-329-78) / 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2022-01-06 | No | No | Historical |