CareOne Acid Relief
- Product NDC
- 41520-392
- 11-digit product format
- 415200392
- Labeler code
- 41520
- Product ID
- 41520-392_b8edc5b9-3ee0-4cf2-b473-a0375155c206
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Sales Company
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2016-06-01
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41520-392-02 | 41520039202 | 1 BOTTLE in 1 CARTON (41520-392-02) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2016-06-01 | 2021-07-31 | No | No | Current |
| 41520-392-09 | 41520039209 | 1 BOTTLE in 1 CARTON (41520-392-09) > 65 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2016-06-01 | 2021-07-31 | No | No | Current |