Maximum Strength Ranitidine
- Product NDC
- 58602-740
- 11-digit product format
- 586020740
- Labeler code
- 58602
- Product ID
- 58602-740_cb84ee80-b612-40be-80a1-1774d10dd814
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aurohealth LLC
- Application
- ANDA207578
- Marketing category
- ANDA
- Marketing start
- 2017-11-13
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 58602-740-16 | 58602074016 | 1 BOTTLE in 1 CARTON (58602-740-16) > 65 TABLET in 1 BOTTLE | 1 bottle | 2017-11-13 | 0000-00-00 | No | No | Current |
| 58602-740-20 | 58602074020 | 1 BOTTLE in 1 CARTON (58602-740-20) > 95 TABLET in 1 BOTTLE | 1 bottle | 2017-11-13 | 0000-00-00 | No | No | Current |
| 58602-740-72 | 58602074072 | 3 BLISTER PACK in 1 CARTON (58602-740-72) > 8 TABLET in 1 BLISTER PACK (58602-740-79) | 3 blister pack | 2017-11-13 | 0000-00-00 | No | No | Current |