heartburn relief
- Product NDC
- 71713-701
- 11-digit product format
- 717130701
- Labeler code
- 71713
- Product ID
- 71713-701_59887b1c-1add-4fe1-a299-e42a1698088e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- THIRTY MADISON INC
- Application
- ANDA077351
- Marketing category
- ANDA
- Marketing start
- 2022-01-11
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71713-701-01 | 71713070101 | 1 BOTTLE in 1 CARTON (71713-701-01) > 85 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2022-01-11 | 0000-00-00 | No | No | Current |