equaline acid reducer
- Product NDC
- 41163-852
- 11-digit product format
- 411630852
- Labeler code
- 41163
- Product ID
- 41163-852_bb00003e-dcdd-408d-af5c-16abd3e67ddb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Supervalu Inc
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2018-03-27
- Marketing end
- 2021-07-31
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 41163-852-62 | 41163085262 | 24 BLISTER PACK in 1 CARTON (41163-852-62) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 24 blister pack | 2018-04-05 | 0000-00-00 | No | No | Current |
| 41163-852-71 | 41163085271 | 1 BOTTLE in 1 CARTON (41163-852-71) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-03-27 | 0000-00-00 | No | No | Current |