ACID REDUCER
- Product NDC
- 68071-5012
- 11-digit product format
- 680715012
- Labeler code
- 68071
- Product ID
- 68071-5012_bbb32fa7-604b-5010-e053-2a95a90ae159
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075294
- Marketing category
- ANDA
- Marketing start
- 2018-10-01
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-5012-3 | 68071501203 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-5012-3) | 2019-08-01 | 0000-00-00 | No | No | Current |